A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16942236



Internal ID28839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156189657..156189657hg38UCSC Ensembl
chr3:155907446..155907446hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5402907
Supporting Variants
Samples
Known GenesKCNAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16942236
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.009887


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