A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14031943



Internal ID4033759
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625404
Supporting Variants
SamplesHG01694
Known GenesTEAD1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14031943
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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