A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891957



Internal ID18839667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:27063816..27240740hg38UCSC Ensembl
Outerchr11:27063816..27240740hg38UCSC Ensembl
Innerchr11:27085363..27262287hg19UCSC Ensembl
Outerchr11:27085363..27262287hg19UCSC Ensembl
Innerchr11:27041939..27218863hg18UCSC Ensembl
Outerchr11:27041939..27218863hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38176925
hg19176925
hg18176925
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788991
Samples
Known GenesBBOX1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891957
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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