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nsv5536764

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:70

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 95 SVs from 24 studies. See in: genome view    
Submitted genomic36,756,884-36,756,953Question Mark
Overlapping variant regions from other studies: 95 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):37,152,928-37,152,997Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5536764Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2236,756,88436,756,953
nsv5536764RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2237,152,92837,152,997

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17728799deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17728799Submitted genomicNC_000022.11:g.367
56884_36756953del
GRCh38 (hg38)NC_000022.11Chr2236,756,88436,756,953
nssv17728799RemappedPerfectNC_000022.10:g.371
52928_37152997del
GRCh37.p13First PassNC_000022.10Chr2237,152,92837,152,997

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)
nssv177287990.002116404
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