A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751544



Internal ID12638410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101496174..101834274hg38UCSC Ensembl
Innerchr15:102036377..102374477hg19UCSC Ensembl
Innerchr15:99853900..100192000hg18UCSC Ensembl
Innerchr15:99853900..100192000hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38338101
hg19338101
hg18338101
hg17338101
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv113e55
Supporting Variantsessv6988894, essv6987164, essv6987165, essv6985124, essv6985123
SamplesSPC_100
Known GenesOR4F15, 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)esv2751544
Frequency
Sample Size771
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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