A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16946534



Internal ID31724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:21205498..21244814hg38UCSC Ensembl
chr4:21207121..21246437hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3839317
hg1939317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5452872
Supporting Variants
Samples
Known GenesKCNIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16946534
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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