A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16909544



Internal ID7142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15982872..15983164hg38UCSC Ensembl
chr2:16122994..16123286hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5448943
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16909544
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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