A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621683



Internal ID7008551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122710359..122712931hg38UCSC Ensembl
Innerchr9:122710385..122712906hg38UCSC Ensembl
Outerchr9:122710334..122712957hg38UCSC Ensembl
chr9:125472638..125475210hg19UCSC Ensembl
Innerchr9:125472664..125475185hg19UCSC Ensembl
Outerchr9:125472613..125475236hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg382573
hg192573
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13618331
SamplesHG02133
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621683
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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