A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984274



Internal ID12630035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22037966..22133812hg38UCSC Ensembl
Innerchr15:22325917..22421763hg19UCSC Ensembl
Innerchr15:19827281..19923127hg18UCSC Ensembl
Innerchr15:19827281..19923127hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3895847
hg1995847
hg1895847
hg1795847
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751353
Supporting Variants
SamplesBEC_683
Known GenesLOC727924, OR4M2, OR4N3P, OR4N4
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984274
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