U.S. flag

An official website of the United States government

nsv5

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:42,759

Genome View

Select assembly:
Overlapping variant regions from other studies: 227 SVs from 65 studies. See in: genome view    
Remapped(Score: Perfect):96,822,040-96,864,798Question Mark
Overlapping variant regions from other studies: 227 SVs from 65 studies. See in: genome view    
Remapped(Score: Perfect):96,451,352-96,494,110Question Mark
Overlapping variant regions from other studies: 4 SVs from 4 studies. See in: genome view    
Submitted genomic96,096,003-96,138,761Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv5RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr796,822,04096,864,798
nsv5RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr796,451,35296,494,110
nsv5Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000007.11Chr796,096,00396,138,761

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv5deletionSAMN00000376SequencingPaired-end mapping297

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv5RemappedPerfectNC_000007.14:g.(96
822040_?)_(?_96864
798)del
GRCh38.p12First PassNC_000007.14Chr796,822,04096,864,798
nssv5RemappedPerfectNC_000007.13:g.(96
451352_?)_(?_96494
110)del
GRCh37.p13First PassNC_000007.13Chr796,451,35296,494,110
nssv5Submitted genomicNC_000007.11:g.(96
096003_?)_(?_96138
761)del9140
NCBI35 (hg17)NC_000007.11Chr796,096,00396,138,761

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