A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14357859



Internal ID22273924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72663727..72664391hg38UCSC Ensembl
chr11:72374771..72375435hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38665
hg19665
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3219486
Supporting Variants
SamplesNA19239
Known GenesPDE2A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14357859
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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