A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985320



Internal ID12636451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90245652..90454197hg38UCSC Ensembl
Innerchr15:90788884..90997429hg19UCSC Ensembl
Innerchr15:88589888..88798433hg18UCSC Ensembl
Innerchr15:88589888..88798433hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38208546
hg19208546
hg18208546
hg17208546
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)essv6985320
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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