A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981827



Internal ID12627305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31604809..32149432hg38UCSC Ensembl
Innerchr15:31897012..32441633hg19UCSC Ensembl
Innerchr15:29684304..30228925hg18UCSC Ensembl
Innerchr15:29684304..30228925hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38544624
hg19544622
hg18544622
hg17544622
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751530
Supporting Variants
SamplesBEC_491
Known GenesCHRNA7, OTUD7A
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981827
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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