A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710330



Internal ID18661925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:20741060..20846701hg38UCSC Ensembl
Innerchr12:20893994..20999635hg19UCSC Ensembl
Innerchr12:20785261..20890902hg18UCSC Ensembl
Cytoband12p12.2
Allele length
AssemblyAllele length
hg38105642
hg19105642
hg18105642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051454
Supporting Variants
Samples
Known GenesSLCO1B3, SLCO1C1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3710330
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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