A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988433



Internal ID12972467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57351455..57485891hg38UCSC Ensembl
Innerchr15:57643653..57778089hg19UCSC Ensembl
Innerchr15:55430945..55565381hg18UCSC Ensembl
Innerchr15:55430945..55565381hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38134437
hg19134437
hg18134437
hg17134437
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751536
Supporting Variants
SamplesBEC_312
Known GenesCGNL1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988433
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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