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nsv5433078

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,393

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 253 SVs from 19 studies. See in: genome view    
Submitted genomic105,887,097-105,888,489Question Mark
Overlapping variant regions from other studies: 253 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):105,131,090-105,132,482Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5433078Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX105,887,097105,888,489
nsv5433078RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX105,131,090105,132,482

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17741806deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17741806Submitted genomicNC_000023.11:g.105
887097_105888489de
l
GRCh38 (hg38)NC_000023.11ChrX105,887,097105,888,489
nssv17741806RemappedPerfectNC_000023.10:g.105
131090_105132482de
l
GRCh37.p13First PassNC_000023.10ChrX105,131,090105,132,482

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)
nssv17741806<0.00116404
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