A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099611



Internal ID22008844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129143072..129143072hg38UCSC Ensembl
chr11:129012967..129012967hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600425
Samples
Known GenesARHGAP32
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099611
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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