A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987497



Internal ID12631031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:29953651..30313633hg38UCSC Ensembl
Innerchr15:30245854..30605836hg19UCSC Ensembl
Innerchr15:28033146..28393128hg18UCSC Ensembl
Innerchr15:28033146..28393128hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38359983
hg19359983
hg18359983
hg17359983
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751527
Supporting Variants
SamplesBEC_779
Known GenesDKFZP434L187, GOLGA8J, GOLGA8T, ULK4P1, ULK4P2, ULK4P3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987497
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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