U.S. flag

An official website of the United States government

nsv5432502

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:40,936

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 402 SVs from 65 studies. See in: genome view    
Submitted genomic17,336,327-17,377,262Question Mark
Overlapping variant regions from other studies: 402 SVs from 65 studies. See in: genome view    
Remapped(Score: Perfect):17,662,822-17,703,757Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5432502Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr117,336,32717,377,262
nsv5432502RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr117,662,82217,703,757

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16899908duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16899908Submitted genomicNC_000001.11:g.173
36327_17377262dup
GRCh38 (hg38)NC_000001.11Chr117,336,32717,377,262
nssv16899908RemappedPerfectNC_000001.10:g.176
62822_17703757dup
GRCh37.p13First PassNC_000001.10Chr117,662,82217,703,757

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)
nssv16899908<0.00116404
Support Center