A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068038



Internal ID20635078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36057214..36057836hg38UCSC Ensembl
chr20:34645136..34645758hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38623
hg19623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6532186
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068038
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00017


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