U.S. flag

An official website of the United States government

nsv8357

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:68,516

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 83 SVs from 13 studies. See in: genome view    
Remapped(Score: Perfect):63,871,003-63,939,518Question Mark
Overlapping variant regions from other studies: 83 SVs from 13 studies. See in: genome view    
Remapped(Score: Perfect):64,783,560-64,852,075Question Mark
Submitted genomic64,946,114-65,014,629Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv8357RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr863,871,00363,939,518
nsv8357RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr864,783,56064,852,075
nsv8357Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000008.9Chr864,946,11465,014,629

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv19737copy number lossNA19132Oligo aCGHProbe signal intensity684

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv19737RemappedPerfectNC_000008.11:g.(63
871003_63934192)_(
63937963_63939518)
del
GRCh38.p12First PassNC_000008.11Chr863,871,00363,934,19263,937,96363,939,518
nssv19737RemappedPerfectNC_000008.10:g.(64
783560_64846749)_(
64850520_64852075)
del
GRCh37.p13First PassNC_000008.10Chr864,783,56064,846,74964,850,52064,852,075
nssv19737Submitted genomicNC_000008.9:g.(649
46114_65009303)_(6
5013074_65014629)d
el
NCBI35 (hg17)NC_000008.9Chr864,946,11465,009,30365,013,07465,014,629

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

Support Center