U.S. flag

An official website of the United States government

nsv5324959

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,109

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 183 SVs from 41 studies. See in: genome view    
Submitted genomic172,315,268-172,321,376Question Mark
Overlapping variant regions from other studies: 183 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):173,179,996-173,186,104Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5324959Submitted genomicGRCh38.p13Primary AssemblyNC_000002.12Chr2172,315,268172,321,376
nsv5324959RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2173,179,996173,186,104

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16766312line1 deletionSequencingSplit read and paired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16766312Submitted genomicNC_000002.12:g.172
315268_172321376de
l
GRCh38.p13NC_000002.12Chr2172,315,268172,321,376
nssv16766312RemappedPerfectNC_000002.11:g.173
179996_173186104de
l
GRCh37.p13First PassNC_000002.11Chr2173,179,996173,186,104

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)
nssv167663120.243
Support Center