A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942032



Internal ID22717463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:84221034..84234222hg38UCSC Ensembl
chr13:84795169..84808357hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3813189
hg1913189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376076
Samples
Known GenesLINC00333
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5942032
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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