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nsv5420174

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:265

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 281 SVs from 16 studies. See in: genome view    
Submitted genomic14,703,523-14,703,787Question Mark
Overlapping variant regions from other studies: 282 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):14,721,645-14,721,909Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5420174Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX14,703,52314,703,787
nsv5420174RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX14,721,64514,721,909

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17739371duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17739371Submitted genomicNC_000023.11:g.147
03523_14703787dup
GRCh38 (hg38)NC_000023.11ChrX14,703,52314,703,787
nssv17739371RemappedPerfectNC_000023.10:g.147
21645_14721909dup
GRCh37.p13First PassNC_000023.10ChrX14,721,64514,721,909

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)
nssv17739371<0.00126404
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