A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572298



Internal ID16359707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:34024926..34218490hg38UCSC Ensembl
Innerchr16:33827393..34020957hg19UCSC Ensembl
Innerchr16:33734894..33928458hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38193565
hg19193565
hg18193565
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5067n54
Supporting Variantsnssv856106
Samples
Known GenesLINC00273
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572298
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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