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nsv5545782

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,785

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 180 SVs from 38 studies. See in: genome view    
Submitted genomic43,120,725-43,128,509Question Mark
Overlapping variant regions from other studies: 180 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):43,516,731-43,524,515Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5545782Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2243,120,72543,128,509
nsv5545782RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2243,516,73143,524,515

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17729295deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17729295Submitted genomicNC_000022.11:g.431
20725_43128509del
GRCh38 (hg38)NC_000022.11Chr2243,120,72543,128,509
nssv17729295RemappedPerfectNC_000022.10:g.435
16731_43524515del
GRCh37.p13First PassNC_000022.10Chr2243,516,73143,524,515

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)
nssv17729295<0.00116404
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