A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483119



Internal ID21140672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77474209..77507493hg38UCSC Ensembl
chr13:78048344..78081628hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3833285
hg1933285
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180199
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483119
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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