A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14176035



Internal ID2436977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60677909..60678333hg38UCSC Ensembl
Innerchr11:60677909..60678333hg38UCSC Ensembl
Outerchr11:60677909..60678333hg38UCSC Ensembl
chr11:60445382..60445806hg19UCSC Ensembl
Innerchr11:60445382..60445806hg19UCSC Ensembl
Outerchr11:60445382..60445806hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38425
hg19425
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626563
Supporting Variants
SamplesHG02147
Known GenesLINC00301
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14176035
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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