A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442818



Internal ID21100371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4560601..4670000hg38UCSC Ensembl
chr11:4581831..4691230hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38109400
hg19109400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991727
Samples
Known GenesC11orf40, OR51D1, OR51E1, OR52I1, OR52I2, TRIM68
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442818
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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