A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1894n209



Internal ID22827969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65084132..65795958hg38UCSC Ensembl
chr7:64544510..65260945hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38711827
hg19716436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5918237, nsv5920709, nsv5922394, nsv5907866
Samples
Known GenesCCT6P1, INTS4L2, LOC441242, SNORA22, ZNF92
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1894n209
Frequency
Sample Size914
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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