A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16946607



Internal ID31764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:21957328..21957403hg38UCSC Ensembl
chr4:21958951..21959026hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140807
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16946607
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.008523


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