A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3533035



Internal ID22402353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47831930..47832297hg38UCSC Ensembl
chr19:48335187..48335554hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14291577, nssv14291578
SamplesNA19239, NA19240
Known GenesCRX
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3533035
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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