A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627914



Internal ID6668058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121033147..121043272hg38UCSC Ensembl
Innerchr11:121033147..121043272hg38UCSC Ensembl
Outerchr11:121032936..121043325hg38UCSC Ensembl
chr11:120903856..120913981hg19UCSC Ensembl
Innerchr11:120903856..120913981hg19UCSC Ensembl
Outerchr11:120903645..120914034hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3810126
hg1910126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14295220
SamplesHG03258
Known GenesTBCEL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627914
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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