A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3259n223



Internal ID22806227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:82294456..82681841hg38UCSC Ensembl
chr17:80252332..80639717hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38387386
hg19387386
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6533313, nsv6532965
Samples
Known GenesC17orf62, CD7, FOXK2, HEXDC, NARF, OGFOD3, RAB40B, SECTM1, TEX19, UTS2R, WDR45B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3259n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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