A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528487



Internal ID22397875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107564090..107564924hg38UCSC Ensembl
chr9:110326371..110327205hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38835
hg19835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14348272
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528487
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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