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nsv5499785

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:394

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 108 SVs from 30 studies. See in: genome view    
Submitted genomic42,490,165-42,490,558Question Mark
Overlapping variant regions from other studies: 108 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):42,782,363-42,782,756Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5499785Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1542,490,16542,490,558
nsv5499785RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1542,782,36342,782,756

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17699786deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17699786Submitted genomicNC_000015.10:g.424
90165_42490558del
GRCh38 (hg38)NC_000015.10Chr1542,490,16542,490,558
nssv17699786RemappedPerfectNC_000015.9:g.4278
2363_42782756del
GRCh37.p13First PassNC_000015.9Chr1542,782,36342,782,756

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)
nssv176997860.002136404
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