A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046570



Internal ID98858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61641232..61648202hg38UCSC Ensembl
chr11:61408704..61415674hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg386971
hg196971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5496398
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046570
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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