A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3219493



Internal ID22364501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94768882..94769200hg38UCSC Ensembl
chr8:95781110..95781428hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14342812
SamplesHG00731
Known GenesDPY19L4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3219493
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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