A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14224071



Internal ID3500040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87967173..87973148hg38UCSC Ensembl
Innerchr11:87967201..87973121hg38UCSC Ensembl
Outerchr11:87967146..87973176hg38UCSC Ensembl
chr11:87678065..87684040hg19UCSC Ensembl
Innerchr11:87678093..87684013hg19UCSC Ensembl
Outerchr11:87678038..87684068hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg385976
hg195976
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627138
Supporting Variants
SamplesHG03108
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14224071
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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