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nsv5417713

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:276,089

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 688 SVs from 56 studies. See in: genome view    
Submitted genomic13,809,400-14,085,488Question Mark
Overlapping variant regions from other studies: 689 SVs from 56 studies. See in: genome view    
Remapped(Score: Perfect):13,827,519-14,103,607Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5417713Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX13,809,40014,085,488
nsv5417713RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX13,827,51914,103,607

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17739334duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17739334Submitted genomicNC_000023.11:g.138
09400_14085488dup
GRCh38 (hg38)NC_000023.11ChrX13,809,40014,085,488
nssv17739334RemappedPerfectNC_000023.10:g.138
27519_14103607dup
GRCh37.p13First PassNC_000023.10ChrX13,827,51914,103,607

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)
nssv17739334<0.00114785
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