A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751291



Internal ID12638157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101764926..101853274hg38UCSC Ensembl
Innerchr15:102305129..102393477hg19UCSC Ensembl
Innerchr15:100122652..100211000hg18UCSC Ensembl
Innerchr15:100122652..100211000hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3888349
hg1988349
hg1888349
hg1788349
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6981761, essv6981760
SamplesBEC_335
Known GenesOR4F13P, OR4F15, OR4F6
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2751291
Frequency
Sample Size771
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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