A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978083



Internal ID12631916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31729405..32219307hg38UCSC Ensembl
Innerchr15:32021608..32511508hg19UCSC Ensembl
Innerchr15:29808900..30298800hg18UCSC Ensembl
Innerchr15:29808900..30298800hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38489903
hg19489901
hg18489901
hg17489901
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35123
Supporting Variants
SamplesNA11830
Known GenesCHRNA7
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978083
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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