A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360904



Internal ID21018457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129690732..129711939hg38UCSC Ensembl
chr3:129409575..129430782hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3821208
hg1921208
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208944
Samples
Known GenesTMCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360904
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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