A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13608726



Internal ID5537032
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621572
Supporting Variants
SamplesNA19000
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13608726
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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