A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17695258



Internal ID118924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20211743..20276391hg38UCSC Ensembl
chr14:20679902..20744550hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3864649
hg1964649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512098
Supporting Variants
Samples
Known GenesOR11H4, OR11H6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17695258
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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