A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494162



Internal ID21151715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76729420..76753931hg38UCSC Ensembl
chr13:77303555..77328066hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3824512
hg1924512
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189522
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494162
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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