A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16909651



Internal ID7209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:8152149..8152388hg38UCSC Ensembl
chr2:8292279..8292518hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446421
Supporting Variants
Samples
Known GenesLINC00299
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16909651
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004371


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