A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490263



Internal ID21147816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95762929..96776023hg38UCSC Ensembl
chr13:96415183..97428277hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381013095
hg191013095
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190915
Samples
Known GenesDNAJC3, HS6ST3, UGGT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490263
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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