A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13601554



Internal ID5828763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111261597..111273986hg38UCSC Ensembl
Innerchr9:111261634..111273949hg38UCSC Ensembl
Outerchr9:111261560..111274023hg38UCSC Ensembl
chr9:114023877..114036266hg19UCSC Ensembl
Innerchr9:114023914..114036229hg19UCSC Ensembl
Outerchr9:114023840..114036303hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3812390
hg1912390
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621486
Supporting Variants
SamplesNA19204
Known GenesMIR7702
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13601554
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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