A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3505086



Internal ID18456681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66975498..67157406hg38UCSC Ensembl
Innerchr10:68735256..68917164hg19UCSC Ensembl
Innerchr10:68405262..68587170hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38181909
hg19181909
hg18181909
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037547
Supporting Variants
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)nssv3505086
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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