A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737113



Internal ID160779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:97872551..97872658hg38UCSC Ensembl
chrX:97127549..97127656hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5423426
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737113
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001562


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