A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983900



Internal ID12977372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54586656..54926183hg38UCSC Ensembl
Innerchr11:51192824..51532624hg19UCSC Ensembl
Innerchr11:51049400..51389200hg18UCSC Ensembl
Innerchr11:51049400..51389200hg17UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38339528
hg19339801
hg18339801
hg17339801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751029
Supporting Variants
SamplesBEC_730
Known GenesOR4A5, OR4C46
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983900
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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