A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029290



Internal ID18771822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:10858971..11406627hg38UCSC Ensembl
Innerchr5:10859083..11406739hg19UCSC Ensembl
Innerchr5:10912083..11459739hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38547657
hg19547657
hg18547657
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5570n100
Supporting Variantsnssv3748677, nssv3748676
Samples
Known GenesCTNND2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029290
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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