A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571431



Internal ID16012154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:9095667..9148663hg38UCSC Ensembl
Innerchr16:9189524..9242520hg19UCSC Ensembl
Innerchr16:9097025..9150021hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3852997
hg1952997
hg1852997
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150525
SamplesHGDP00515
Known GenesC16orf72
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571431
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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