A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16909031



Internal ID6812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9088640..9302101hg38UCSC Ensembl
chr2:9228769..9442230hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38213462
hg19213462
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446916
Supporting Variants
Samples
Known GenesASAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16909031
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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