U.S. flag

An official website of the United States government

nsv6145080

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:200,715

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1262 SVs from 85 studies. See in: genome view    
Submitted genomic32,150,486-32,351,200Question Mark
Overlapping variant regions from other studies: 1269 SVs from 87 studies. See in: genome view    
Remapped(Score: Perfect):32,161,807-32,362,521Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6145080Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1632,150,48632,351,200
nsv6145080RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1632,161,80732,362,521

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17707346deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17707346Submitted genomicNC_000016.10:g.321
50486_32351200del
GRCh38 (hg38)NC_000016.10Chr1632,150,48632,351,200
nssv17707346RemappedPerfectNC_000016.9:g.3216
1807_32362521del
GRCh37.p13First PassNC_000016.9Chr1632,161,80732,362,521

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)
nssv177073460.018935308
Support Center