A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477288



Internal ID21134841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112655770..112672014hg38UCSC Ensembl
chr13:113310084..113326328hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3816245
hg1916245
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194217
Samples
Known GenesC13orf35
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477288
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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