A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528052



Internal ID20901413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36607463..36620882hg38UCSC Ensembl
chr20:35235866..35249285hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3813420
hg1913420
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202218
Samples
Known GenesC20orf24, SLA2, TGIF2-C20orf24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528052
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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