A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419456



Internal ID21077009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17157233..17161001hg38UCSC Ensembl
chr8:17014742..17018510hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg383769
hg193769
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220450
Samples
Known GenesZDHHC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419456
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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