A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737131



Internal ID160797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:98679022..98679073hg38UCSC Ensembl
chrX:97934020..97934071hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556187
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737131
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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