A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546106



Internal ID15986829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:41525974..41529795hg38UCSC Ensembl
Innerchr1:41991645..41995466hg19UCSC Ensembl
Innerchr1:41764232..41768053hg18UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg383822
hg193822
hg183822
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv251n54
Supporting Variantsnssv712654, nssv712653
Samples
Known GenesHIVEP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546106
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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