A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367805



Internal ID21025358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:17699715..17702365hg38UCSC Ensembl
chr3:17741207..17743857hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg382651
hg192651
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211487
Samples
Known GenesTBC1D5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367805
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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