A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480727



Internal ID21138280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:80327320..80328123hg38UCSC Ensembl
chr13:80901455..80902258hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38804
hg19804
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190148
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480727
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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