A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477293



Internal ID21134846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:93113557..93121906hg38UCSC Ensembl
chr13:93765810..93774159hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg388350
hg198350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015288
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477293
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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