A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980556



Internal ID12635950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90104756..90235099hg38UCSC Ensembl
Innerchr15:90647988..90778331hg19UCSC Ensembl
Innerchr15:88448992..88579335hg18UCSC Ensembl
Innerchr15:88448992..88579335hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38130344
hg19130344
hg18130344
hg17130344
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34892
Supporting Variants
SamplesNA19209
Known GenesCIB1, GDPGP1, SEMA4B
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980556
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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