A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978407



Internal ID12635234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90109664..90249264hg38UCSC Ensembl
Innerchr15:90652896..90792496hg19UCSC Ensembl
Innerchr15:88453900..88593500hg18UCSC Ensembl
Innerchr15:88453900..88593500hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38139601
hg19139601
hg18139601
hg17139601
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34677
Supporting Variants
SamplesNA19093
Known GenesCIB1, GDPGP1, SEMA4B
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978407
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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