A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047925



Internal ID99815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63232987..63233226hg38UCSC Ensembl
chr11:63000459..63000698hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5504722
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047925
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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