A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14360465



Internal ID22284865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64914641..64920647hg38UCSC Ensembl
chr11:64682113..64688119hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg386007
hg196007
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3215223
Supporting Variants
SamplesNA19239
Known GenesATG2A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14360465
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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