A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16911305



Internal ID8306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26398039..26425785hg38UCSC Ensembl
chr2:26620907..26648653hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3827747
hg1927747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449309
Supporting Variants
Samples
Known GenesDRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16911305
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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