A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981829



Internal ID12627303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31729407..32219354hg38UCSC Ensembl
Innerchr15:32021610..32511555hg19UCSC Ensembl
Innerchr15:29808902..30298847hg18UCSC Ensembl
Innerchr15:29808902..30298847hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38489948
hg19489946
hg18489946
hg17489946
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751530
Supporting Variants
SamplesBEC_491
Known GenesCHRNA7
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981829
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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