A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435323



Internal ID21092876
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 StatusM
Merged Variants
Supporting Variantsnssv18230464
Samples
Known GenesVDAC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435323
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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