A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5526253



Internal ID8503656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:111588767..111589529hg38UCSC Ensembl
Outerchr9:111588610..111589682hg38UCSC Ensembl
Innerchr9:114351047..114351809hg19UCSC Ensembl
Outerchr9:114350890..114351962hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg381073
hg191073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672152
Supporting Variants
SamplesNA18988
Known GenesPTGR1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5526253
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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