A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14358785



Internal ID22196837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86025337..86025610hg38UCSC Ensembl
chr11:85736379..85736652hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3225350
Supporting Variants
SamplesHG00731
Known GenesPICALM
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14358785
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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