A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621496



Internal ID6661675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111825752..111827859hg38UCSC Ensembl
Innerchr9:111825802..111827809hg38UCSC Ensembl
Outerchr9:111825680..111827931hg38UCSC Ensembl
chr9:114588032..114590139hg19UCSC Ensembl
Innerchr9:114588082..114590089hg19UCSC Ensembl
Outerchr9:114587960..114590211hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg382108
hg192108
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13602707
SamplesNA19225
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621496
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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