A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039479



Internal ID19128698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:7818125..7964473hg38UCSC Ensembl
Innerchr12:7970721..8117069hg19UCSC Ensembl
Innerchr12:7861988..8008336hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38146349
hg19146349
hg18146349
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1352n100
Supporting Variantsnssv3505967
Samples
Known GenesSLC2A14, SLC2A3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039479
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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