A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571250



Internal ID16358659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3153034..3192615hg38UCSC Ensembl
Innerchr16:3203035..3242615hg19UCSC Ensembl
Innerchr16:3143036..3182616hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3839582
hg1939581
hg1839581
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4874n54
Supporting Variantsnssv1148906
SamplesHGDP00615
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571250
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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