A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17991663



Internal ID20558703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4449872..4656651hg38UCSC Ensembl
chr11:4471102..4677881hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38206780
hg19206780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438415
Supporting Variants
Samples
Known GenesC11orf40, OR51D1, OR51E1, OR52I1, OR52I2, OR52K1, OR52K2, OR52M1, TRIM68
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17991663
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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