A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230464



Internal ID20797504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42403431..42407496hg38UCSC Ensembl
chr8:42260949..42265014hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg384066
hg194066
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435323
Supporting Variants
Samples
Known GenesVDAC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230464
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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