A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433008



Internal ID21090561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:79281139..79295806hg38UCSC Ensembl
chr8:80193374..80208041hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3814668
hg1914668
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227858
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433008
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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