A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202253



Internal ID20769293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39226944..39248500hg38UCSC Ensembl
chr20:37855587..37877143hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3821557
hg1921557
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531555
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202253
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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