A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369099



Internal ID21026652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49246130..49248073hg38UCSC Ensembl
chr3:49283563..49285506hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381944
hg191944
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209355
Samples
Known GenesCCDC36
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369099
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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