A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740416



Internal ID164082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:65947654..65947790hg38UCSC Ensembl
chrX:65167496..65167632hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432470
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740416
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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