A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621616



Internal ID7008484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:118077409..118084483hg38UCSC Ensembl
Innerchr9:118077415..118084477hg38UCSC Ensembl
Outerchr9:118077403..118084489hg38UCSC Ensembl
chr9:120839687..120846761hg19UCSC Ensembl
Innerchr9:120839693..120846755hg19UCSC Ensembl
Outerchr9:120839681..120846767hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg387075
hg197075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13612635
SamplesHG01556
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621616
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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