A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571435



Internal ID16358844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:9231230..9274839hg38UCSC Ensembl
Innerchr16:9325087..9368696hg19UCSC Ensembl
Innerchr16:9232588..9276197hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3843610
hg1943610
hg1843610
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150527
SamplesHGDP00535
Known GenesMIR548X
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571435
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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