A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740578



Internal ID164244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:69783787..69800625hg38UCSC Ensembl
chrX:69003631..69020469hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3816839
hg1916839
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422329
Supporting Variants
Samples
Known GenesEDA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740578
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000208117


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