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nsv5517581

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:168,626

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 856 SVs from 81 studies. See in: genome view    
Submitted genomic38,296,000-38,464,625Question Mark
Overlapping variant regions from other studies: 864 SVs from 81 studies. See in: genome view    
Remapped(Score: Good):36,924,402-37,093,268Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5517581Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2038,296,00038,464,625
nsv5517581RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2036,924,40237,093,268

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17732299duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17732299Submitted genomicNC_000020.11:g.382
96000_38464625dup
GRCh38 (hg38)NC_000020.11Chr2038,296,00038,464,625
nssv17732299RemappedGoodNC_000020.10:g.369
24402_37093268dup
GRCh37.p13First PassNC_000020.10Chr2036,924,40237,093,268

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)
nssv17732299<0.00116404
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