A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13559438



Internal ID3561254
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621085
Supporting Variants
SamplesNA20507
Known GenesCENPP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13559438
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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