A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531555



Internal ID20904916
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 StatusM
Merged Variants
Supporting Variantsnssv18202253
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531555
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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