U.S. flag

An official website of the United States government

nsv5479490

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:134,950

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1827 SVs from 106 studies. See in: genome view    
Submitted genomic6,619,706-6,754,655Question Mark
Overlapping variant regions from other studies: 1830 SVs from 106 studies. See in: genome view    
Remapped(Score: Perfect):6,619,706-6,754,655Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5479490Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr96,619,7066,754,655
nsv5479490RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr96,619,7066,754,655

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17019677duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17019677Submitted genomicNC_000009.12:g.661
9706_6754655dup
GRCh38 (hg38)NC_000009.12Chr96,619,7066,754,655
nssv17019677RemappedPerfectNC_000009.11:g.661
9706_6754655dup
GRCh37.p13First PassNC_000009.11Chr96,619,7066,754,655

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)Allele Count (AC)Allele Number (AN)
nssv17019677<0.00166404
Support Center