A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488709



Internal ID21146262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:53657601..53664400hg38UCSC Ensembl
chr13:54231736..54238535hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1836n223
Supporting Variantsnssv18187925
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488709
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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