A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416648



Internal ID21074201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42389701..42395400hg38UCSC Ensembl
chr8:42247219..42252918hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221638
Samples
Known GenesVDAC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416648
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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