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nsv5425679

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:83,279

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 372 SVs from 43 studies. See in: genome view    
Submitted genomic65,592,748-65,676,026Question Mark
Overlapping variant regions from other studies: 372 SVs from 43 studies. See in: genome view    
Remapped(Score: Good):64,812,628-64,895,887Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5425679Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX65,592,74865,676,026
nsv5425679RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX64,812,62864,895,887

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17740400duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17740400Submitted genomicNC_000023.11:g.655
92748_65676026dup
GRCh38 (hg38)NC_000023.11ChrX65,592,74865,676,026
nssv17740400RemappedGoodNC_000023.10:g.648
12628_64895887dup
GRCh37.p13First PassNC_000023.10ChrX64,812,62864,895,887

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)
nssv17740400<0.00144799
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