A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482528



Internal ID21140081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97432701..97434100hg38UCSC Ensembl
chr13:98084955..98086354hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186304
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482528
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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