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nsv5555911

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:70

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 274 SVs from 22 studies. See in: genome view    
Submitted genomic46,592,209-46,592,278Question Mark
Overlapping variant regions from other studies: 274 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):46,451,644-46,451,713Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5555911Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX46,592,20946,592,278
nsv5555911RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX46,451,64446,451,713

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17736758alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17736758Submitted genomicNC_000023.11:g.465
92209_46592278ins1
02
GRCh38 (hg38)NC_000023.11ChrX46,592,20946,592,278
nssv17736758RemappedPerfectNC_000023.10:g.464
51644_46451713ins1
02
GRCh37.p13First PassNC_000023.10ChrX46,451,64446,451,713

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)
nssv177367580.008526404
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