A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483512



Internal ID21141065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112961414..112965457hg38UCSC Ensembl
chr13:113615728..113619771hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg384044
hg194044
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007302
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483512
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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