A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982797



Internal ID12628872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101496174..101765274hg38UCSC Ensembl
Innerchr15:102036377..102305477hg19UCSC Ensembl
Innerchr15:99853900..100123000hg18UCSC Ensembl
Innerchr15:99853900..100123000hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38269101
hg19269101
hg18269101
hg17269101
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751545
Supporting Variants
SamplesBEC_594
Known GenesTARSL2, TM2D3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982797
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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