A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493972



Internal ID21151525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20211746..20276405hg38UCSC Ensembl
chr14:20679905..20744564hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3864660
hg1964660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016538
Samples
Known GenesOR11H4, OR11H6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493972
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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