A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983195



Internal ID12628289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44715242..44861115hg38UCSC Ensembl
Innerchr10:45210690..45356563hg19UCSC Ensembl
Innerchr10:44530696..44676569hg18UCSC Ensembl
Innerchr10:44530696..44676569hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38145874
hg19145874
hg18145874
hg17145874
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750895
Supporting Variants
SamplesBEC_554
Known GenesTMEM72-AS1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983195
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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