A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627327



Internal ID6667475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94717955..94726723hg38UCSC Ensembl
Innerchr11:94717985..94726693hg38UCSC Ensembl
Outerchr11:94717925..94726753hg38UCSC Ensembl
chr11:94451121..94459889hg19UCSC Ensembl
Innerchr11:94451151..94459859hg19UCSC Ensembl
Outerchr11:94451091..94459919hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg388769
hg198769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14241845, essv14241844
SamplesHG03760, HG03711
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627327
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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