A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424436



Internal ID21081989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94882401..94986400hg38UCSC Ensembl
chr8:95894629..95998628hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38104000
hg19104000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224251
Samples
Known GenesCCNE2, TP53INP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424436
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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