A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427125



Internal ID21084678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9648001..9669500hg38UCSC Ensembl
chr8:9505511..9527010hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3821500
hg1921500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230272
Samples
Known GenesTNKS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427125
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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