A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740417



Internal ID164083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:65972489..65972603hg38UCSC Ensembl
chrX:65192331..65192445hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415677
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740417
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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