U.S. flag

An official website of the United States government

nsv5555893

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:110

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 91 SVs from 23 studies. See in: genome view    
Submitted genomic94,232,385-94,232,494Question Mark
Overlapping variant regions from other studies: 91 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):94,626,161-94,626,270Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5555893Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1294,232,38594,232,494
nsv5555893RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1294,626,16194,626,270

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17684179inversionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17684179Submitted genomicNC_000012.12:g.942
32385_94232494inv
GRCh38 (hg38)NC_000012.12Chr1294,232,38594,232,494
nssv17684179RemappedPerfectNC_000012.11:g.946
26161_94626270inv
GRCh37.p13First PassNC_000012.11Chr1294,626,16194,626,270

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)
nssv17684179<0.00146404
Support Center