A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621489



Internal ID7008358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111491527..111493521hg38UCSC Ensembl
Innerchr9:111491535..111493514hg38UCSC Ensembl
Outerchr9:111491520..111493529hg38UCSC Ensembl
chr9:114253807..114255801hg19UCSC Ensembl
Innerchr9:114253815..114255794hg19UCSC Ensembl
Outerchr9:114253800..114255809hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg381995
hg191995
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13602047, essv13602046, essv13602049, essv13602050, essv13602043, essv13602044, essv13602045, essv13602041, essv13602048, essv13602042
SamplesNA21097, HG03738, HG03645, NA20896, HG04020, HG04047, HG03805, HG01880, HG04177, HG03824
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621489
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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