A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279614



Internal ID20488832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:42447082..42447082hg38UCSC Ensembl
chr2:42674222..42674222hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755733
Supporting Variants
Samples
Known GenesKCNG3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279614
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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