A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492448



Internal ID21150001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113482740..113529446hg38UCSC Ensembl
chr13:114137055..114183761hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3846707
hg1946707
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181753
Samples
Known GenesDCUN1D2, TMCO3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492448
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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