A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191016



Internal ID20758056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128812462..129027216hg38UCSC Ensembl
chr11:128682357..128897111hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38214755
hg19214755
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471155
Supporting Variants
Samples
Known GenesARHGAP32, C11orf45, FLI1, KCNJ1, KCNJ5, TP53AIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191016
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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