A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13602707



Internal ID3604523
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621496
Supporting Variants
SamplesNA19225
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13602707
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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