A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545147



Internal ID16332556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:4332451..4343712hg38UCSC Ensembl
Innerchr1:4392511..4403772hg19UCSC Ensembl
Innerchr1:4292371..4303632hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3811262
hg1911262
hg1811262
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv60n54
Supporting Variantsnssv708918
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545147
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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