A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626490



Internal ID7013322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56666942..56671730hg38UCSC Ensembl
chr11:56434418..56439206hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg384789
hg194789
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14168336, essv14168337, essv14168339, essv14168338, essv14168340
SamplesHG00351, NA21109, NA20770, HG02088, NA18643
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626490
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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