A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16917259



Internal ID12252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:82337086..82340277hg38UCSC Ensembl
chr2:82564210..82567401hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg383192
hg193192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5439109
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16917259
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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