A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484329



Internal ID21141882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41950510..41959743hg38UCSC Ensembl
chr13:42524646..42533879hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg389234
hg199234
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195876
Samples
Known GenesVWA8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484329
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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