A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3228586



Internal ID22370726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17349132..17349226hg38UCSC Ensembl
chr19:17459941..17460035hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4166n152
Supporting Variantsnssv14286283
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3228586
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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