A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486653



Internal ID21144206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:61323601..61344100hg38UCSC Ensembl
chr13:61897734..61918233hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3820500
hg1920500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194390
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486653
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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