A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3534717



Internal ID22403992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17593100..17593474hg38UCSC Ensembl
chr19:17703909..17704283hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14286309, nssv14286307, nssv14286308
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3534717
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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