A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039951



Internal ID19129170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:20727483..20788304hg38UCSC Ensembl
Innerchr12:20880417..20941238hg19UCSC Ensembl
Innerchr12:20771684..20832505hg18UCSC Ensembl
Cytoband12p12.2
Allele length
AssemblyAllele length
hg3860822
hg1960822
hg1860822
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710329
Samples
Known GenesSLCO1C1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039951
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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