A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7291n223



Internal ID22810259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18126977..18248912hg38UCSC Ensembl
chr8:17984486..18106421hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38121936
hg19121936
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6423716, nsv6425264
Samples
Known GenesNAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7291n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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