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nsv5426844

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:166,175

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 533 SVs from 50 studies. See in: genome view    
Submitted genomic66,548,026-66,714,200Question Mark
Overlapping variant regions from other studies: 533 SVs from 50 studies. See in: genome view    
Remapped(Score: Perfect):65,767,868-65,934,042Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5426844Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX66,548,02666,714,200
nsv5426844RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX65,767,86865,934,042

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17740437duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17740437Submitted genomicNC_000023.11:g.665
48026_66714200dup
GRCh38 (hg38)NC_000023.11ChrX66,548,02666,714,200
nssv17740437RemappedPerfectNC_000023.10:g.657
67868_65934042dup
GRCh37.p13First PassNC_000023.10ChrX65,767,86865,934,042

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)
nssv177404370.00164805
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