A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621640



Internal ID7008508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:119880812..119886053hg38UCSC Ensembl
Innerchr9:119880818..119886047hg38UCSC Ensembl
Outerchr9:119880806..119886059hg38UCSC Ensembl
chr9:122643090..122648331hg19UCSC Ensembl
Innerchr9:122643096..122648325hg19UCSC Ensembl
Outerchr9:122643084..122648337hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg385242
hg195242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13613202, essv13613203
SamplesHG02325, HG01577
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621640
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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