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nsv5881610

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:390

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 867 SVs from 27 studies. See in: genome view    
Submitted genomic770,849-771,238Question Mark
Overlapping variant regions from other studies: 868 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):731,584-731,973Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5881610Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX770,849771,238
nsv5881610RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX731,584731,973

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17469613duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17469613Submitted genomicNC_000023.11:g.770
849_771238dup
GRCh38 (hg38)NC_000023.11ChrX770,849771,238
nssv17469613RemappedPerfectNC_000023.10:g.731
584_731973dup
GRCh37.p13First PassNC_000023.10ChrX731,584731,973

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)
nssv174696130.0811134
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