A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16912488



Internal ID9078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38755374..38755647hg38UCSC Ensembl
chr2:38982516..38982789hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451011
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16912488
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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