A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987218



Internal ID12636452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90245664..90440464hg38UCSC Ensembl
Innerchr15:90788896..90983696hg19UCSC Ensembl
Innerchr15:88589900..88784700hg18UCSC Ensembl
Innerchr15:88589900..88784700hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38194801
hg19194801
hg18194801
hg17194801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751541
Supporting Variants
SamplesSPC_141
Known GenesCIB1, GABARAPL3, IQGAP1, NGRN, TTLL13, ZNF774
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987218
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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