A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463229



Internal ID21120782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117080713..117081389hg38UCSC Ensembl
chr11:116951429..116952105hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987133
Samples
Known GenesSIK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463229
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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