A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625404



Internal ID6665551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:12906001..12907110hg38UCSC Ensembl
Innerchr11:12906033..12907079hg38UCSC Ensembl
Outerchr11:12905970..12907142hg38UCSC Ensembl
chr11:12927548..12928657hg19UCSC Ensembl
Innerchr11:12927580..12928626hg19UCSC Ensembl
Outerchr11:12927517..12928689hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381110
hg191110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14031942, essv14031941, essv14031943
SamplesHG01083, HG01079, HG01694
Known GenesTEAD1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625404
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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