A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528483



Internal ID22397871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75383647..75383767hg38UCSC Ensembl
chr9:77998563..77998683hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9603n152
Supporting Variantsnssv14346290, nssv14346289
SamplesNA19239, HG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528483
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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