A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519401



Internal ID20892762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20827558..20828174hg38UCSC Ensembl
chr20:20808201..20808817hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38617
hg19617
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203209
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519401
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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