A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479411



Internal ID21136964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79274080..79274400hg38UCSC Ensembl
chr13:79848215..79848535hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012837
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479411
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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