A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv491e215



Internal ID22786001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97998739..97999161hg38UCSC Ensembl
chr9:100761021..100761443hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3545178, esv3545179
Samples
Known GenesANP32B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)dgv491e215
Frequency
Sample Size767
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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