A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16925886



Internal ID18010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:214496242..214496245hg38UCSC Ensembl
chr2:215360966..215360969hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5550814
Supporting Variants
Samples
Known GenesVWC2L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16925886
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.218594


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