A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981761



Internal ID12625954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101800274..101853274hg38UCSC Ensembl
Innerchr15:102340477..102393477hg19UCSC Ensembl
Innerchr15:100158000..100211000hg18UCSC Ensembl
Innerchr15:100158000..100211000hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3853001
hg1953001
hg1853001
hg1753001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751291
Supporting Variants
SamplesBEC_335
Known GenesOR4F13P, OR4F15, OR4F6
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981761
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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