A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16913887



Internal ID10010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62460339..62465208hg38UCSC Ensembl
chr2:62687474..62692343hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg384870
hg194870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446897
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16913887
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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