A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13559428



Internal ID3561244
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621078
Supporting Variants
SamplesHG02820
Known GenesCENPP, NOL8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13559428
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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