A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3504574



Internal ID18456169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66630592..66920330hg38UCSC Ensembl
Innerchr10:68390350..68680088hg19UCSC Ensembl
Innerchr10:68060356..68350094hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38289739
hg19289739
hg18289739
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038079
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)nssv3504574
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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