A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603192



Internal ID16043915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:57353638..60409841hg38UCSC Ensembl
Innerchr6:57218436..57381883hg19UCSC Ensembl
Innerchr6:57326395..57489842hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg383056204
hg19163448
hg18163448
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10677n54
Supporting Variantsnssv1060930
Samples
Known GenesPRIM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603192
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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