A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787423



Internal ID19167411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:94304801..94326356hg38UCSC Ensembl
Innerchr11:94037967..94059522hg19UCSC Ensembl
Innerchr11:93677615..93699170hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3821556
hg1921556
hg1821556
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892073
Supporting Variants
Samples
Known GenesFOLR4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787423
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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