A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784262



Internal ID18819810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:94175706..94215699hg38UCSC Ensembl
Innerchr11:93908872..93948865hg19UCSC Ensembl
Innerchr11:93548520..93588513hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3839994
hg1939994
hg1839994
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=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784262
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer