A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085964



Internal ID20653004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:33667697..33682120hg38UCSC Ensembl
chr2:33892764..33907187hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3814424
hg1914424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6343630
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085964
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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