A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18082575



Internal ID20649615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207346101..207348500hg38UCSC Ensembl
chr2:208210825..208213224hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6352980
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18082575
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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