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nsv883637

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,965

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1534 SVs from 96 studies. See in: genome view    
Remapped(Score: Perfect):29,889,309-29,905,273Question Mark
Overlapping variant regions from other studies: 650 SVs from 37 studies. See in: genome view    
Remapped(Score: Pass):1,152,239-1,161,607Question Mark
Overlapping variant regions from other studies: 1535 SVs from 97 studies. See in: genome view    
Remapped(Score: Perfect):29,857,086-29,873,050Question Mark
Overlapping variant regions from other studies: 650 SVs from 37 studies. See in: genome view    
Remapped(Score: Pass):1,157,859-1,167,227Question Mark
Overlapping variant regions from other studies: 656 SVs from 29 studies. See in: genome view    
Submitted genomic29,965,065-29,981,029Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv883637RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr629,889,30929,890,18829,904,76529,905,273
nsv883637RemappedPassGRCh38.p12ALT_REF_LOCI_4Second PassNT_167246.2Chr6|NT_16
7246.2		-1,152,2391,161,6071,161,607
nsv883637RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr629,857,08629,857,96529,872,54229,873,050
nsv883637RemappedPassGRCh37.p13ALT_REF_LOCI_4Second PassNT_167246.1Chr6|NT_16
7246.1		-1,157,8591,167,2271,167,227
nsv883637Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000006.10Chr629,965,06529,965,94429,980,52129,981,029

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1530019copy number gainMS10169SNP arraySNP genotyping analysis10

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1530019RemappedPassNT_167246.2:g.(?_1
152239)_(1161607_1
161607)dup		GRCh38.p12Second PassNT_167246.2Chr6|NT_16
7246.2		-1,152,2391,161,6071,161,607
nssv1530019RemappedPerfectNC_000006.12:g.(29
889309_29890188)_(
29904765_29905273)
dup		GRCh38.p12First PassNC_000006.12Chr629,889,30929,890,18829,904,76529,905,273
nssv1530019RemappedPassNT_167246.1:g.(?_1
157859)_(1167227_1
167227)dupNT_16724
6.1:g.(?_1157859)_
(1167227_1167227)d
up		GRCh37.p13Second PassNT_167246.1Chr6|NT_16
7246.1		-1,157,8591,167,2271,167,227
nssv1530019RemappedPerfectNC_000006.11:g.(29
857086_29857965)_(
29872542_29873050)
dup		GRCh37.p13First PassNC_000006.11Chr629,857,08629,857,96529,872,54229,873,050
nssv1530019Submitted genomicNC_000006.10:g.(29
965065_29965944)_(
29980521_29981029)
dup		NCBI36 (hg18)NC_000006.10Chr629,965,06529,965,94429,980,52129,981,029

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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