A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421797



Internal ID21079350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22351530..22520784hg38UCSC Ensembl
chr8:22209043..22378297hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38169255
hg19169255
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222018
Samples
Known GenesPIWIL2, PPP3CC, SLC39A14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421797
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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