A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978406



Internal ID12635235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90079820..90245676hg38UCSC Ensembl
Innerchr15:90623052..90788908hg19UCSC Ensembl
Innerchr15:88424056..88589912hg18UCSC Ensembl
Innerchr15:88424056..88589912hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38165857
hg19165857
hg18165857
hg17165857
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34677
Supporting Variants
SamplesNA19093
Known GenesCIB1, GDPGP1, IDH2, SEMA4B, ZNF710
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978406
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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