A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17519295



Internal ID21843654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:42447083..42447083hg38UCSC Ensembl
chr2:42674223..42674223hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6056010
Supporting Variants
Samples
Known GenesKCNG3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17519295
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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