A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17044141



Internal ID97164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33970184..33973325hg38UCSC Ensembl
chr11:33991731..33994872hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg383142
hg193142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5499126
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17044141
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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