A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203297



Internal ID20770337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34031846..34032524hg38UCSC Ensembl
chr20:32619652..32620330hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38679
hg19679
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533042
Supporting Variants
Samples
Known GenesRALY
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203297
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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