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nsv5512947

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:71

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 125 SVs from 22 studies. See in: genome view    
Submitted genomic37,584,535-37,584,605Question Mark
Overlapping variant regions from other studies: 125 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):38,158,672-38,158,742Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5512947Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1337,584,53537,584,605
nsv5512947RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1338,158,67238,158,742

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17686956deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17686956Submitted genomicNC_000013.11:g.375
84535_37584605del
GRCh38 (hg38)NC_000013.11Chr1337,584,53537,584,605
nssv17686956RemappedPerfectNC_000013.10:g.381
58672_38158742del
GRCh37.p13First PassNC_000013.10Chr1338,158,67238,158,742

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)
nssv17686956<0.00116404
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