A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18084193



Internal ID20651233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:226187370..226198615hg38UCSC Ensembl
chr2:227052086..227063331hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3811246
hg1911246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6343103
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18084193
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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