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nsv5422356

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,947

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 246 SVs from 27 studies. See in: genome view    
Submitted genomic73,628,700-73,636,646Question Mark
Overlapping variant regions from other studies: 246 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):72,848,535-72,856,481Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5422356Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX73,628,70073,636,646
nsv5422356RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX72,848,53572,856,481

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17740728deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17740728Submitted genomicNC_000023.11:g.736
28700_73636646del
GRCh38 (hg38)NC_000023.11ChrX73,628,70073,636,646
nssv17740728RemappedPerfectNC_000023.10:g.728
48535_72856481del
GRCh37.p13First PassNC_000023.10ChrX72,848,53572,856,481

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)
nssv177407280.004184805
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