A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012793



Internal ID19102010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:51819521..51884244hg38UCSC Ensembl
Innerchr4:52685687..52750410hg19UCSC Ensembl
Innerchr4:52380444..52445167hg18UCSC Ensembl
Cytoband4q11
Allele length
AssemblyAllele length
hg3864724
hg1964724
hg1864724
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3625258
Samples
Known GenesDCUN1D4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012793
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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