A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223715



Internal ID22367402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9845252..9845377hg38UCSC Ensembl
chr19:9955928..9956053hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14285962
SamplesHG00512
Known GenesPIN1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223715
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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