A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068032



Internal ID20635072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35951223..35953039hg38UCSC Ensembl
chr20:34539145..34540961hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381817
hg191817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533835
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068032
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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