A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3510841



Internal ID18809122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66489541..66776296hg38UCSC Ensembl
Innerchr10:68249299..68536054hg19UCSC Ensembl
Innerchr10:67919305..68206060hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38286756
hg19286756
hg18286756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048376
Supporting Variants
Samples
Known GenesCTNNA3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3510841
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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