A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475428



Internal ID21132981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59744589..59751805hg38UCSC Ensembl
chr11:59512062..59519278hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg387217
hg197217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992468
Samples
Known GenesOR10V2P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475428
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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