A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18081563



Internal ID20648603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:19264846..19326397hg38UCSC Ensembl
chr2:19464607..19526158hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3861552
hg1961552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6338102
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18081563
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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