A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621486



Internal ID7008355
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13601554, essv13601553, essv13601555
SamplesNA19204, HG03169, NA19835
Known GenesMIR7702
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621486
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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