A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012416



Internal ID19101633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:67495820..67565107hg38UCSC Ensembl
Innerchr3:67546244..67615531hg19UCSC Ensembl
Innerchr3:67628934..67698221hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3869288
hg1969288
hg1869288
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593968
Samples
Known GenesSUCLG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012416
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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