A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603084



Internal ID16390493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:49461993..49478796hg38UCSC Ensembl
Innerchr6:49429706..49446509hg19UCSC Ensembl
Innerchr6:49537665..49554468hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3816804
hg1916804
hg1816804
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10655n54
Supporting Variantsnssv1058821
Samples
Known GenesCENPQ, MUT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603084
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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