A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987168



Internal ID12982831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19798855..19879145hg38UCSC Ensembl
Innerchr14:20267014..20347304hg19UCSC Ensembl
Innerchr14:19336854..19417144hg18UCSC Ensembl
Innerchr14:19336854..19417144hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3880291
hg1980291
hg1880291
hg1780291
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34399
Supporting Variants
SamplesSPC_102
Known GenesOR4K2, OR4N2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987168
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