A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6861n223



Internal ID22809829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65035202..65870265hg38UCSC Ensembl
chr7:64495580..65335252hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38835064
hg19839673
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6616341, nsv6619355
Samples
Known GenesCCT6P1, CCT6P3, INTS4L2, LOC441242, SNORA22, ZNF92
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6861n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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