A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471155



Internal ID21128708
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 StatusM
Merged Variants
Supporting Variantsnssv18191016
Samples
Known GenesARHGAP32, C11orf45, FLI1, KCNJ1, KCNJ5, TP53AIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471155
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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