A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627704



Internal ID7014532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:109525949..109530154hg38UCSC Ensembl
chr11:109396675..109400880hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg384206
hg194206
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14280550, essv14280534, essv14280552, essv14280539, essv14280549, essv14280540, essv14280546, essv14280531, essv14280538, essv14280554, essv14280543, essv14280532, essv14280558, essv14280529, essv14280542, essv14280544, essv14280559, essv14280555, essv14280545, essv14280560, essv14280525, essv14280541, essv14280528, essv14280527, essv14280557, essv14280548, essv14280526, essv14280553, essv14280556, essv14280547, essv14280551, essv14280535, essv14280537, essv14280536, essv14280533, essv14280530
SamplesHG03514, HG03366, NA19914, NA19819, NA20356, NA18510, NA19198, HG02860, NA19138, NA19904, HG02505, NA20412, HG03394, HG03132, NA18933, NA19913, HG03428, HG03575, NA18871, HG03123, NA19114, HG03388, HG02884, NA19099, HG02635, HG02594, HG03109, HG01990, NA18909, HG03539, HG01915, HG02314, HG03473, NA19468, HG03470, NA19463
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627704
Frequency
Sample Size2504
Observed Gain0
Observed Loss36
Observed Complex0
Frequencyn/a


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