A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528770



Internal ID22398161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36474249..36475082hg38UCSC Ensembl
chr9:36474246..36475079hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38834
hg19834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14346485
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528770
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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