A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068052



Internal ID20635092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36501211..36523767hg38UCSC Ensembl
chr20:35129614..35152170hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3822557
hg1922557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522669
Supporting Variants
Samples
Known GenesDLGAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068052
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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