A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988247



Internal ID12980788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81627999..81718113hg38UCSC Ensembl
Innerchr11:81339041..81429155hg19UCSC Ensembl
Innerchr11:81016689..81106803hg18UCSC Ensembl
Innerchr11:81016689..81106803hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3890115
hg1990115
hg1890115
hg1790115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34835
Supporting Variants
SamplesNA18633
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988247
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