A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483100



Internal ID21140653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20916778..20923950hg38UCSC Ensembl
chr13:21490917..21498089hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg387173
hg197173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007693
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483100
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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