A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17991396



Internal ID20558436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4431253..4550337hg38UCSC Ensembl
chr11:4452483..4571567hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38119085
hg19119085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441701
Supporting Variants
Samples
Known GenesOR52K1, OR52K2, OR52M1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17991396
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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