A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17042603



Internal ID96111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22813734..23250368hg38UCSC Ensembl
chr11:22835280..23271914hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38436635
hg19436635
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5495901
Supporting Variants
Samples
Known GenesCCDC179, SVIP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17042603
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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