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nsv5424004

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:286

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 300 SVs from 21 studies. See in: genome view    
Submitted genomic19,345,383-19,345,668Question Mark
Overlapping variant regions from other studies: 301 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):19,363,501-19,363,786Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5424004Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX19,345,38319,345,668
nsv5424004RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX19,363,50119,363,786

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17739529deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17739529Submitted genomicNC_000023.11:g.193
45383_19345668del
GRCh38 (hg38)NC_000023.11ChrX19,345,38319,345,668
nssv17739529RemappedPerfectNC_000023.10:g.193
63501_19363786del
GRCh37.p13First PassNC_000023.10ChrX19,363,50119,363,786

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)
nssv17739529<0.00116404
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