A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621572



Internal ID7008440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:115473132..115478630hg38UCSC Ensembl
Innerchr9:115473132..115478630hg38UCSC Ensembl
Outerchr9:115473004..115478706hg38UCSC Ensembl
chr9:118235411..118240909hg19UCSC Ensembl
Innerchr9:118235411..118240909hg19UCSC Ensembl
Outerchr9:118235283..118240985hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg385499
hg195499
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13608725, essv13608726, essv13608727, essv13608728, essv13608724
SamplesNA19055, NA18988, NA19315, NA18986, NA19000
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621572
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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