A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14362265



Internal ID22301492
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3558062
Supporting Variants
SamplesNA19240
Known GenesARHGAP32
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14362265
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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