A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483208



Internal ID21140761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32308401..32320800hg38UCSC Ensembl
chr13:32882538..32894937hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3812400
hg1912400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193597
Samples
Known GenesBRCA2, ZAR1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483208
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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