A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526301



Internal ID20899662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37058518..37074433hg38UCSC Ensembl
chr20:35686921..35702836hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3815916
hg1915916
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202226
Samples
Known GenesRBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526301
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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