A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3558062



Internal ID22426865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129143072..129145383hg38UCSC Ensembl
chr11:129012967..129015278hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg382312
hg192312
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14362265, nssv14362264, nssv14362263
SamplesNA19239, NA19240, HG00513
Known GenesARHGAP32
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3558062
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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