A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494510



Internal ID21152063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27146251..27148603hg38UCSC Ensembl
chr13:27720388..27722740hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg382353
hg192353
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194177
Samples
Known GenesUSP12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494510
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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