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nsv1156683

  • Variant Calls:29
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,400

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 285 SVs from 66 studies. See in: genome view    
Remapped(Score: Perfect):67,164,253-67,182,652Question Mark
Overlapping variant regions from other studies: 285 SVs from 66 studies. See in: genome view    
Submitted genomic66,629,240-66,647,639Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv1156683RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nsv1156683Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr766,629,24066,629,32966,645,23266,647,639

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv4021243deletionSNP arraySNP genotyping analysis1
nssv4021244deletionSNP arraySNP genotyping analysis1
nssv4021245deletionSNP arraySNP genotyping analysis1
nssv4021246deletionSNP arraySNP genotyping analysis1
nssv4021247deletionSNP arraySNP genotyping analysis1
nssv4021248deletionSNP arraySNP genotyping analysis1
nssv4021249deletionSNP arraySNP genotyping analysis1
nssv4021250deletionSNP arraySNP genotyping analysis1
nssv4021252deletionSNP arraySNP genotyping analysis1
nssv4021253deletionSNP arraySNP genotyping analysis1
nssv4021254deletionSNP arraySNP genotyping analysis1
nssv4021255duplicationSNP arraySNP genotyping analysis3
nssv4021256deletionSNP arraySNP genotyping analysis1
nssv4021257deletionSNP arraySNP genotyping analysis1
nssv4021258deletionSNP arraySNP genotyping analysis1
nssv4021259deletionSNP arraySNP genotyping analysis1
nssv4021260deletionSNP arraySNP genotyping analysis1
nssv4021261deletionSNP arraySNP genotyping analysis1
nssv4021263deletionSNP arraySNP genotyping analysis1
nssv4021264deletionSNP arraySNP genotyping analysis1
nssv4021265deletionSNP arraySNP genotyping analysis1
nssv4021266deletionSNP arraySNP genotyping analysis0
nssv4021267deletionSNP arraySNP genotyping analysis1
nssv4021268deletionSNP arraySNP genotyping analysis1
nssv4021269deletionSNP arraySNP genotyping analysis1
nssv4021270deletionSNP arraySNP genotyping analysis1
nssv4021271deletionSNP arraySNP genotyping analysis0
nssv4021272deletionSNP arraySNP genotyping analysis1
nssv4021274deletionSNP arraySNP genotyping analysis1

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv4021243RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021244RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021245RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021246RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021247RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021248RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021249RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021250RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021252RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021253RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021254RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021255RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
dup
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021256RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021257RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021258RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021259RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021260RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021261RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021263RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021264RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021265RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021266RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021267RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021268RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021269RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021270RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021271RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021272RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021274RemappedPerfectNC_000007.14:g.(67
164253_67164342)_(
67180245_67182652)
del
GRCh38.p12First PassNC_000007.14Chr767,164,25367,164,34267,180,24567,182,652
nssv4021243Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021244Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021245Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021246Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021247Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021248Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021249Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021250Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021252Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021253Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021254Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021255Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
dup
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021256Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021257Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021258Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021259Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021260Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021261Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021263Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021264Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021265Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021266Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021267Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021268Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021269Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021270Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021271Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021272Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639
nssv4021274Submitted genomicNC_000007.13:g.(66
629240_66629329)_(
66645232_66647639)
del
GRCh37 (hg19)NC_000007.13Chr766,629,24066,629,32966,645,23266,647,639

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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