A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936132



Internal ID22711483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20215229..20248715hg38UCSC Ensembl
chr14:20683388..20716874hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3833487
hg1933487
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376746
Samples
Known GenesOR11H4, OR11H6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936132
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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