A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3531086



Internal ID22400450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:22652221..22652388hg38UCSC Ensembl
chr19:22835023..22835190hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14287852, nssv14287853
SamplesHG00732, HG00733
Known GenesZNF492
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3531086
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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