A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362392



Internal ID21019945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:17574687..17604406hg38UCSC Ensembl
chr3:17616179..17645898hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3829720
hg1929720
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211457
Samples
Known GenesTBC1D5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362392
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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