A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751532



Internal ID12638398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31716805..32219354hg38UCSC Ensembl
Innerchr15:32009008..32511555hg19UCSC Ensembl
Innerchr15:29796300..30298847hg18UCSC Ensembl
Innerchr15:29796300..30298847hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38502550
hg19502548
hg18502548
hg17502548
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv109e55
Supporting Variantsessv6985961, essv6985960, essv6988967, essv6985959, essv6985958
SamplesSPC_88
Known GenesCHRNA7
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)esv2751532
Frequency
Sample Size771
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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