A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982798



Internal ID12628871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101496193..101853034hg38UCSC Ensembl
Innerchr15:102036396..102393237hg19UCSC Ensembl
Innerchr15:99853919..100210760hg18UCSC Ensembl
Innerchr15:99853919..100210760hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38356842
hg19356842
hg18356842
hg17356842
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751545
Supporting Variants
SamplesBEC_594
Known GenesOR4F13P, OR4F15, OR4F6, TARSL2, TM2D3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982798
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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