A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483719



Internal ID21141272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:63369001..63404000hg38UCSC Ensembl
chr13:63943134..63978133hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3835000
hg1935000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1870n223
Supporting Variantsnssv18179484
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483719
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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