A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986609



Internal ID12635230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90104764..90245664hg38UCSC Ensembl
Innerchr15:90647996..90788896hg19UCSC Ensembl
Innerchr15:88449000..88589900hg18UCSC Ensembl
Innerchr15:88449000..88589900hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38140901
hg19140901
hg18140901
hg17140901
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34677
Supporting Variants
SamplesNA19093
Known GenesCIB1, GDPGP1, SEMA4B
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986609
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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