A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528094



Internal ID22397479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23549706..23550346hg38UCSC Ensembl
chr8:23407219..23407859hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38641
hg19641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14341020, nssv14341019
SamplesNA19238, HG00513
Known GenesSLC25A37
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528094
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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