A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621085



Internal ID6661266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92596234..92609536hg38UCSC Ensembl
Innerchr9:92596234..92609536hg38UCSC Ensembl
Outerchr9:92595734..92610036hg38UCSC Ensembl
chr9:95358516..95371818hg19UCSC Ensembl
Innerchr9:95358516..95371818hg19UCSC Ensembl
Outerchr9:95358016..95372318hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3813303
hg1913303
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13559438
SamplesNA20507
Known GenesCENPP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621085
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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