A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891995



Internal ID18839705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:49134487..49221694hg38UCSC Ensembl
Outerchr11:49134487..49221694hg38UCSC Ensembl
Innerchr11:49156039..49243246hg19UCSC Ensembl
Outerchr11:49156039..49243246hg19UCSC Ensembl
Innerchr11:49112615..49199822hg18UCSC Ensembl
Outerchr11:49112615..49199822hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg3887208
hg1987208
hg1887208
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789856
Samples
Known GenesFOLH1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891995
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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