A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17688429



Internal ID112095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102366401..102366745hg38UCSC Ensembl
chr11:102237132..102237476hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512251
Supporting Variants
Samples
Known GenesBIRC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17688429
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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