A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892073



Internal ID19186469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:94304801..94326356hg38UCSC Ensembl
Outerchr11:94304801..94326356hg38UCSC Ensembl
Innerchr11:94037967..94059522hg19UCSC Ensembl
Outerchr11:94037967..94059522hg19UCSC Ensembl
Innerchr11:93677615..93699170hg18UCSC Ensembl
Outerchr11:93677615..93699170hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3821556
hg1921556
hg1821556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787423
Samples
Known GenesFOLR4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892073
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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