A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16914947



Internal ID10723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63659681..63668109hg38UCSC Ensembl
chr2:63886815..63895243hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg388429
hg198429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5453052
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16914947
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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