A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468566



Internal ID21126119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111473251..111473970hg38UCSC Ensembl
chr11:111343976..111344695hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38720
hg19720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986760
Samples
Known GenesBTG4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468566
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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