A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16910804



Internal ID7972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16895049..16895049hg38UCSC Ensembl
chr2:17076316..17076316hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534097
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16910804
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.009522


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