A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13609791



Internal ID2780421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116853913..116935591hg38UCSC Ensembl
Innerchr9:116853913..116935591hg38UCSC Ensembl
Outerchr9:116853413..116936091hg38UCSC Ensembl
chr9:119616192..119697870hg19UCSC Ensembl
Innerchr9:119616192..119697870hg19UCSC Ensembl
Outerchr9:119615692..119698370hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3881679
hg1981679
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621603
Supporting Variants
SamplesHG02455
Known GenesASTN2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13609791
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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