A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936787



Internal ID22712146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:43681590..43681639hg38UCSC Ensembl
chr13:44255726..44255775hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370940
Samples
Known GenesENOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936787
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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