A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365120



Internal ID21022673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46700160..46703538hg38UCSC Ensembl
chr3:46741650..46745028hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg383379
hg193379
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209284
Samples
Known GenesTMIE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365120
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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