A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485201



Internal ID21142754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60395901..60398200hg38UCSC Ensembl
chr13:60970035..60972334hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184357
Samples
Known GenesTDRD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485201
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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