A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529584



Internal ID22398976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:88014562..88014640hg38UCSC Ensembl
chr8:89026790..89026868hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14342010, nssv14342011, nssv14342012
SamplesNA19239, HG00732, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529584
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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