A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625687



Internal ID7012521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:25030443..25038076hg38UCSC Ensembl
Innerchr11:25030443..25038076hg38UCSC Ensembl
Outerchr11:25029943..25038576hg38UCSC Ensembl
chr11:25051989..25059622hg19UCSC Ensembl
Innerchr11:25051989..25059622hg19UCSC Ensembl
Outerchr11:25051489..25060122hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg387634
hg197634
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14061901, essv14061900
SamplesHG01441, NA12889
Known GenesLUZP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625687
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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