A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050214



Internal ID18792745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66771920..66946821hg38UCSC Ensembl
Innerchr10:68531678..68706579hg19UCSC Ensembl
Innerchr10:68201684..68376585hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38174902
hg19174902
hg18174902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3519505
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)nsv1050214
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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