A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16924583



Internal ID17144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215706279..215706308hg38UCSC Ensembl
chr2:216571002..216571031hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5550608
Supporting Variants
Samples
Known GenesLINC00607
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16924583
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.009366


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