A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047896



Internal ID99794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63028600..63035356hg38UCSC Ensembl
chr11:62796072..62802828hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg386757
hg196757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501324
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047896
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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