A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740335



Internal ID164001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:63824209..63831135hg38UCSC Ensembl
chrX:63044089..63051015hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg386927
hg196927
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415638
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740335
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.016025


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