A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914591



Internal ID22689808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134528657..134566306hg38UCSC Ensembl
chr7:134213409..134251058hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3837650
hg1937650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1922n209
Supporting Variantsnssv17434666
Samples
Known GenesAKR1B10, AKR1B15
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914591
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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