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nsv5540702

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,548

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 179 SVs from 38 studies. See in: genome view    
Submitted genomic36,270,315-36,271,862Question Mark
Overlapping variant regions from other studies: 179 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):37,642,613-37,644,160Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5540702Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2136,270,31536,271,862
nsv5540702RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2137,642,61337,644,160

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17726757deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17726757Submitted genomicNC_000021.9:g.3627
0315_36271862del
GRCh38 (hg38)NC_000021.9Chr2136,270,31536,271,862
nssv17726757RemappedPerfectNC_000021.8:g.3764
2613_37644160del
GRCh37.p13First PassNC_000021.8Chr2137,642,61337,644,160

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)
nssv177267570.01676404
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