A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1058822



Internal ID15565322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:49461993..49482628hg38UCSC Ensembl
Innerchr6:49429706..49450341hg19UCSC Ensembl
Innerchr6:49537665..49558300hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3820636
hg1920636
hg1820636
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603085
Supporting Variants
Samples
Known GenesCENPQ, MUT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1058822
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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