A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487861



Internal ID21145414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34982401..34988100hg38UCSC Ensembl
chr13:35556538..35562237hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1800n223
Supporting Variantsnssv18188338
Samples
Known GenesNBEA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487861
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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