A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075845



Internal ID18970818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:20833365..20834566hg38UCSC Ensembl
chr12:20986299..20987500hg19UCSC Ensembl
Cytoband12p12.2
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767677
SamplesKWP1
Known GenesSLCO1B3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075845
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer