A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527233



Internal ID22396619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:51404349..51404587hg38UCSC Ensembl
chr8:52316909..52317147hg19UCSC Ensembl
Cytoband8q11.22
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9166n152
Supporting Variantsnssv14342459, nssv14342458
SamplesNA19238, NA19240
Known GenesPXDNL
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527233
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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