A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050616



Internal ID19139835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:90884096..90920866hg38UCSC Ensembl
Innerchr12:91277873..91314643hg19UCSC Ensembl
Innerchr12:89802004..89838774hg18UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg3836771
hg1936771
hg1836771
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3524821
Samples
Known GenesLINC00615
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050616
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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