A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16925328



Internal ID17632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:142444048..142444057hg38UCSC Ensembl
chr2:143201617..143201626hg19UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534768
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16925328
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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