A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044293



Internal ID18786824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66975498..67158604hg38UCSC Ensembl
Innerchr10:68735256..68918362hg19UCSC Ensembl
Innerchr10:68405262..68588368hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38183107
hg19183107
hg18183107
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv916n100
Supporting Variantsnssv3706100, nssv3503928, nssv3512939
Samples
Known GenesCTNNA3, LRRTM3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044293
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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