A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13579185



Internal ID2460278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98891301..98897333hg38UCSC Ensembl
Innerchr9:98891325..98897309hg38UCSC Ensembl
Outerchr9:98891277..98897357hg38UCSC Ensembl
chr9:101653583..101659615hg19UCSC Ensembl
Innerchr9:101653607..101659591hg19UCSC Ensembl
Outerchr9:101653559..101659639hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg386033
hg196033
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621216
Supporting Variants
SamplesHG02165
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13579185
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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