A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046575



Internal ID98860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61669082..61678498hg38UCSC Ensembl
chr11:61436554..61445970hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg389417
hg199417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513072
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046575
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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