A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783486



Internal ID18829508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:94175706..94228955hg38UCSC Ensembl
Innerchr11:93908872..93962121hg19UCSC Ensembl
Innerchr11:93548520..93601769hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3853250
hg1953250
hg1853250
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892071
Supporting Variants
Samples
Known GenesPANX1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=16
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783486
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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