A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625989



Internal ID7012823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37742851..37820265hg38UCSC Ensembl
chr11:37764401..37841815hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3877415
hg1977415
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv192e214
Supporting Variantsessv14095014, essv14095012, essv14095015, essv14095013, essv14095009, essv14095011, essv14095010
SamplesHG01402, NA20863, NA20796, NA19657, HG02221, HG02314, NA19786
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625989
Frequency
Sample Size2504
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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