A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1922n209



Internal ID22827997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134528657..134566617hg38UCSC Ensembl
chr7:134213409..134251369hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3837961
hg1937961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5914591, nsv5909896, nsv5915429
Samples
Known GenesAKR1B10, AKR1B15
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1922n209
Frequency
Sample Size914
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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