A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18174976



Internal ID20742016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14654998..14655528hg38UCSC Ensembl
chr9:14654996..14655526hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38531
hg19531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425518
Supporting Variants
Samples
Known GenesZDHHC21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18174976
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00032


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