A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626920



Internal ID7013750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:79631587..79637991hg38UCSC Ensembl
Innerchr11:79631587..79637991hg38UCSC Ensembl
Outerchr11:79631337..79638207hg38UCSC Ensembl
chr11:79342631..79349035hg19UCSC Ensembl
Innerchr11:79342631..79349035hg19UCSC Ensembl
Outerchr11:79342381..79349251hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg386405
hg196405
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14216006, essv14216003, essv14216002, essv14216000, essv14216005, essv14216004, essv14216001, essv14215999, essv14215998
SamplesHG01350, HG02144, HG01345, HG03028, NA19256, HG02837, HG03060, HG02462, HG02051
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626920
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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