A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985017



Internal ID12631258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66976136..67178536hg38UCSC Ensembl
Innerchr10:68735894..68938294hg19UCSC Ensembl
Innerchr10:68405900..68608300hg18UCSC Ensembl
Innerchr10:68405900..68608300hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38202401
hg19202401
hg18202401
hg17202401
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750974
Supporting Variants
SamplesBEC_820
Known GenesCTNNA3, LRRTM3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985017
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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