A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625442



Internal ID7012276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15786462..15794738hg38UCSC Ensembl
Innerchr11:15786462..15794738hg38UCSC Ensembl
Outerchr11:15785962..15795238hg38UCSC Ensembl
chr11:15808008..15816284hg19UCSC Ensembl
Innerchr11:15808008..15816284hg19UCSC Ensembl
Outerchr11:15807508..15816784hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg388277
hg198277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14034675, essv14034674, essv14034671, essv14034673, essv14034678, essv14034677, essv14034679, essv14034676, essv14034670, essv14034669, essv14034672
SamplesHG03163, NA19399, HG03300, HG03372, HG02545, HG03270, HG03511, NA18915, HG02557, HG02274, NA19360
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625442
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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