A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478360



Internal ID21135913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:64680001..64741400hg38UCSC Ensembl
chr13:65254133..65315532hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3861400
hg1961400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18010956
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478360
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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