A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627630



Internal ID7014458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106253578..106254398hg38UCSC Ensembl
Innerchr11:106253587..106254390hg38UCSC Ensembl
Outerchr11:106253570..106254407hg38UCSC Ensembl
chr11:106124305..106125125hg19UCSC Ensembl
Innerchr11:106124314..106125117hg19UCSC Ensembl
Outerchr11:106124297..106125134hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38821
hg19821
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14271047, essv14271046
SamplesNA20321, NA20320
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627630
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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