A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13613196



Internal ID5731553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:119529074..119542434hg38UCSC Ensembl
Innerchr9:119529074..119542434hg38UCSC Ensembl
Outerchr9:119528917..119542541hg38UCSC Ensembl
chr9:122291352..122304712hg19UCSC Ensembl
Innerchr9:122291352..122304712hg19UCSC Ensembl
Outerchr9:122291195..122304819hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3813361
hg1913361
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621636
Supporting Variants
SamplesNA19108
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13613196
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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