A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621361



Internal ID6661540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105702189..105703073hg38UCSC Ensembl
Innerchr9:105702191..105703072hg38UCSC Ensembl
Outerchr9:105702188..105703075hg38UCSC Ensembl
chr9:108464470..108465354hg19UCSC Ensembl
Innerchr9:108464472..108465353hg19UCSC Ensembl
Outerchr9:108464469..108465356hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38885
hg19885
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13593264, essv13593272, essv13593265, essv13593261, essv13593267, essv13593270, essv13593269, essv13593268, essv13593271, essv13593262, essv13593266, essv13593263
SamplesNA21100, NA20894, HG03873, NA12348, HG01398, HG01092, NA20765, NA21113, NA21123, NA21102, HG03998, HG01786
Known GenesTMEM38B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621361
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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