A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012024



Internal ID18754560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:48077739..48201180hg38UCSC Ensembl
Innerchr3:48119229..48242670hg19UCSC Ensembl
Innerchr3:48094233..48217674hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38123442
hg19123442
hg18123442
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3595251
Samples
Known GenesCDC25A, MAP4, MIR4443
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012024
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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