A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487564



Internal ID21145117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105297832..105308092hg38UCSC Ensembl
chr13:105950183..105960443hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3810261
hg1910261
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194377
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487564
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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