A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626608



Internal ID6666758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62492487..62497387hg38UCSC Ensembl
Innerchr11:62492487..62497387hg38UCSC Ensembl
Outerchr11:62492182..62497576hg38UCSC Ensembl
chr11:62259959..62264859hg19UCSC Ensembl
Innerchr11:62259959..62264859hg19UCSC Ensembl
Outerchr11:62259654..62265048hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg384901
hg194901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14179702, essv14179700, essv14179701
SamplesNA19372, NA19452, NA19431
Known GenesAHNAK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626608
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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