A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456418



Internal ID21113971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111744872..111748534hg38UCSC Ensembl
chr11:111615596..111619258hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg383663
hg193663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986778
Samples
Known GenesPPP2R1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456418
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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