A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892071



Internal ID18839781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:94179870..94215699hg38UCSC Ensembl
Outerchr11:94175706..94236560hg38UCSC Ensembl
Innerchr11:93913036..93948865hg19UCSC Ensembl
Outerchr11:93908872..93969726hg19UCSC Ensembl
Innerchr11:93552684..93588513hg18UCSC Ensembl
Outerchr11:93548520..93609374hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3860855
hg1960855
hg1860855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799794, essv25783486, essv25784262
Samples
Known GenesPANX1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892071
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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