A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989020



Internal ID12981926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55677818..55800740hg38UCSC Ensembl
Innerchr11:55445294..55568216hg19UCSC Ensembl
Innerchr11:55201870..55324792hg18UCSC Ensembl
Innerchr11:55201870..55324792hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38122923
hg19122923
hg18122923
hg17122923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34793
Supporting Variants
SamplesNA19093
Known GenesOR5D13, OR5D14
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989020
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