A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462083



Internal ID21119636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111755801..111783600hg38UCSC Ensembl
chr11:111626525..111654324hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3827800
hg1927800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194193
Samples
Known GenesALG9, PPP2R1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462083
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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