A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751527



Internal ID12985079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:29953605..30313633hg38UCSC Ensembl
Innerchr15:30245808..30605836hg19UCSC Ensembl
Innerchr15:28033100..28393128hg18UCSC Ensembl
Innerchr15:28033100..28393128hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38360029
hg19360029
hg18360029
hg17360029
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6984122, essv6987497
SamplesBEC_779
Known GenesDKFZP434L187, GOLGA8J, GOLGA8T, ULK4P1, ULK4P2, ULK4P3
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)esv2751527
Frequency
Sample Size771
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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