A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14223503



Internal ID1335136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86927847..86931067hg38UCSC Ensembl
Innerchr11:86928347..86930567hg38UCSC Ensembl
Outerchr11:86926847..86932067hg38UCSC Ensembl
chr11:86638889..86642109hg19UCSC Ensembl
Innerchr11:86639389..86641609hg19UCSC Ensembl
Outerchr11:86637889..86643109hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg383221
hg193221
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627110
Supporting Variants
SamplesHG01176
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14223503
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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