A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3091n223



Internal ID22806059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35822938..36193984hg38UCSC Ensembl
chr17:34149942..34521383hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38371047
hg19371442
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6510305, nsv6501005
Samples
Known GenesC17orf66, CCL14, CCL15, CCL15-CCL14, CCL16, CCL18, CCL23, CCL3, CCL4, CCL5, LYZL6, RDM1, TAF15, TBC1D3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3091n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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