A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984122



Internal ID12631037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:29953605..30313605hg38UCSC Ensembl
Innerchr15:30245808..30605808hg19UCSC Ensembl
Innerchr15:28033100..28393100hg18UCSC Ensembl
Innerchr15:28033100..28393100hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38360001
hg19360001
hg18360001
hg17360001
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)essv6984122
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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