A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17710119



Internal ID133785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65107098..65111691hg38UCSC Ensembl
chr16:65141001..65145594hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg384594
hg194594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5533692
Supporting Variants
Samples
Known GenesCDH11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17710119
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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