A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627367



Internal ID7014197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96098936..96099904hg38UCSC Ensembl
Innerchr11:96098936..96099904hg38UCSC Ensembl
Outerchr11:96098636..96100181hg38UCSC Ensembl
chr11:95832100..95833068hg19UCSC Ensembl
Innerchr11:95832100..95833068hg19UCSC Ensembl
Outerchr11:95831800..95833345hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38969
hg19969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14244103, essv14244101, essv14244100, essv14244108, essv14244104, essv14244102, essv14244098, essv14244107, essv14244099, essv14244105, essv14244106
SamplesNA19909, NA19130, HG03268, NA19024, NA19471, HG03169, HG03397, HG03117, HG02317, HG03313, HG02013
Known GenesMAML2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627367
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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