A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978417



Internal ID12635252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90079820..90245652hg38UCSC Ensembl
Innerchr15:90623052..90788884hg19UCSC Ensembl
Innerchr15:88424056..88589888hg18UCSC Ensembl
Innerchr15:88424056..88589888hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38165833
hg19165833
hg18165833
hg17165833
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34436
Supporting Variants
SamplesNA19094
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)essv6978417
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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