A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481407



Internal ID21138960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113458367..113543203hg38UCSC Ensembl
chr13:114112682..114197518hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3884837
hg1984837
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007760
Samples
Known GenesDCUN1D2, TMCO3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481407
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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