A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6860n223



Internal ID22809828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65035155..65888939hg38UCSC Ensembl
chr7:64495533..65353926hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38853785
hg19858394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6606714, nsv6610802, nsv6601679, nsv6608610
Samples
Known GenesCCT6P1, CCT6P3, INTS4L2, LOC441242, SNORA22, VKORC1L1, ZNF92
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6860n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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