A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208667



Internal ID20775709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43241683..43329733hg38UCSC Ensembl
chr3:43283175..43371225hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3888051
hg1988051
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368242
Supporting Variants
Samples
Known GenesSNRK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208667
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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