A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891996



Internal ID18839706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:49173538..49443281hg38UCSC Ensembl
Outerchr11:49173538..49443281hg38UCSC Ensembl
Innerchr11:49195090..49464833hg19UCSC Ensembl
Outerchr11:49195090..49464833hg19UCSC Ensembl
Innerchr11:49151666..49421409hg18UCSC Ensembl
Outerchr11:49151666..49421409hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38269744
hg19269744
hg18269744
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789015
Samples
Known GenesFOLH1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891996
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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