A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987619



Internal ID12630491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20928395..22300068hg38UCSC Ensembl
Innerchr15:21133724..22588019hg19UCSC Ensembl
Innerchr15:19398383..20089383hg18UCSC Ensembl
Innerchr15:19398383..20089383hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381371674
hg191454296
hg18691001
hg17691001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751354
Supporting Variants
SamplesBEC_718
Known GenesCT60, CXADRP2, LOC646214, LOC727924, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987619
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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