A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920899



Internal ID22696122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85426274..86526514hg38UCSC Ensembl
chr11:85137318..86237556hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381100241
hg191100239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361907
Samples
Known GenesC11orf73, CCDC81, CCDC83, CCDC89, CREBZF, DLG2, EED, ME3, MIR6755, PICALM, SYTL2, TMEM126A, TMEM126B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920899
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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