A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13648202



Internal ID1970749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135109821..135110483hg38UCSC Ensembl
Innerchr9:135109871..135110433hg38UCSC Ensembl
Outerchr9:135109771..135110533hg38UCSC Ensembl
chr9:138001667..138002329hg19UCSC Ensembl
Innerchr9:138001717..138002279hg19UCSC Ensembl
Outerchr9:138001617..138002379hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38663
hg19663
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621975
Supporting Variants
SamplesHG01817
Known GenesOLFM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13648202
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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