A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546158



Internal ID15986881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:45750903..46029762hg38UCSC Ensembl
Innerchr1:46216575..46495434hg19UCSC Ensembl
Innerchr1:45989162..46268021hg18UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38278860
hg19278860
hg18278860
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv712896
Samples
Known GenesMAST2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546158
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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