A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980163



Internal ID12634679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5410754..5447674hg38UCSC Ensembl
Innerchr11:5431984..5468904hg19UCSC Ensembl
Innerchr11:5388560..5425480hg18UCSC Ensembl
Innerchr11:5388560..5425480hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3836921
hg1936921
hg1836921
hg1736921
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34391
Supporting Variants
SamplesNA18966
Known GenesOR51B5, OR51I1, OR51Q1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980163
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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