A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14287852



Internal ID22200887
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3531086
Supporting Variants
SamplesHG00732
Known GenesZNF492
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14287852
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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