A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751545



Internal ID12638411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101496174..101853034hg38UCSC Ensembl
Innerchr15:102036377..102393237hg19UCSC Ensembl
Innerchr15:99853900..100210760hg18UCSC Ensembl
Innerchr15:99853900..100210760hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38356861
hg19356861
hg18356861
hg17356861
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv113e55
Supporting Variantsessv6986263, essv6982797, essv6982798
SamplesBEC_594
Known GenesOR4F13P, OR4F15, OR4F6, TARSL2, TM2D3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2751545
Frequency
Sample Size771
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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