A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484448



Internal ID21142001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:83090801..83227900hg38UCSC Ensembl
chr13:83664936..83802035hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38137100
hg19137100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183114
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484448
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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