A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474533



Internal ID21132086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59713096..59713558hg38UCSC Ensembl
chr11:59480569..59481031hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992466
Samples
Known GenesOR10V1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474533
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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