A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546161



Internal ID16333570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:45845603..46032703hg38UCSC Ensembl
Innerchr1:46311275..46498375hg19UCSC Ensembl
Innerchr1:46083862..46270962hg18UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38187101
hg19187101
hg18187101
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv712898
Samples
Known GenesMAST2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546161
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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