A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14029129



Internal ID2807455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11132964..11140169hg38UCSC Ensembl
Innerchr11:11132964..11140169hg38UCSC Ensembl
Outerchr11:11132464..11140669hg38UCSC Ensembl
chr11:11154511..11161716hg19UCSC Ensembl
Innerchr11:11154511..11161716hg19UCSC Ensembl
Outerchr11:11154011..11162216hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg387206
hg197206
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625371
Supporting Variants
SamplesHG02479
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14029129
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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