A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621078



Internal ID6661259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92320076..92379665hg38UCSC Ensembl
chr9:95082358..95141947hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3859590
hg1959590
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13559428
SamplesHG02820
Known GenesCENPP, NOL8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621078
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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