A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466955



Internal ID21124508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58354641..58388109hg38UCSC Ensembl
chr11:58122114..58155582hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3833469
hg1933469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993717
Samples
Known GenesOR5B17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466955
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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