A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6874n223



Internal ID22809842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65587481..65910200hg38UCSC Ensembl
chr7:65052394..65375187hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38322720
hg19322794
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6611499, nsv6609669
Samples
Known GenesCCT6P1, INTS4L2, LOC441242, SNORA22, VKORC1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6874n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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