A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984373



Internal ID12630202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66976136..67157436hg38UCSC Ensembl
Innerchr10:68735894..68917194hg19UCSC Ensembl
Innerchr10:68405900..68587200hg18UCSC Ensembl
Innerchr10:68405900..68587200hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38181301
hg19181301
hg18181301
hg17181301
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750973
Supporting Variants
SamplesBEC_696
Known GenesCTNNA3, LRRTM3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984373
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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