A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363794



Internal ID21021347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31785939..31813359hg38UCSC Ensembl
chr3:31827431..31854851hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg3827421
hg1927421
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210515
Samples
Known GenesOSBPL10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363794
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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