A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035807



Internal ID18778338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:21011760..21046655hg38UCSC Ensembl
Innerchr12:21164694..21199589hg19UCSC Ensembl
Innerchr12:21055961..21090856hg18UCSC Ensembl
Cytoband12p12.2
Allele length
AssemblyAllele length
hg3834896
hg1934896
hg1834896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710331
Samples
Known GenesSLCO1B7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035807
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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