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nsv5431806

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:648,488

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1351 SVs from 57 studies. See in: genome view    
Submitted genomic15,172,883-15,821,370Question Mark
Overlapping variant regions from other studies: 1353 SVs from 57 studies. See in: genome view    
Remapped(Score: Perfect):15,191,005-15,839,493Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5431806Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX15,172,88315,821,370
nsv5431806RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX15,191,00515,839,493

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17739385duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17739385Submitted genomicNC_000023.11:g.151
72883_15821370dup
GRCh38 (hg38)NC_000023.11ChrX15,172,88315,821,370
nssv17739385RemappedPerfectNC_000023.10:g.151
91005_15839493dup
GRCh37.p13First PassNC_000023.10ChrX15,191,00515,839,493

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)
nssv17739385<0.00144805
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