A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16939339



Internal ID26940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136893179..136893196hg38UCSC Ensembl
chr3:136612021..136612038hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538906
Supporting Variants
Samples
Known GenesNCK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16939339
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.529384


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