A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434081



Internal ID21091634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101200601..101205000hg38UCSC Ensembl
chr8:102212829..102217228hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg384400
hg194400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235083
Samples
Known GenesZNF706
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434081
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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