A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736130



Internal ID159796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3714789..3714952hg38UCSC Ensembl
chrX:3632830..3632993hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555495
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736130
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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