A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571457



Internal ID16358866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11630499..11660598hg38UCSC Ensembl
Innerchr16:11724355..11754454hg19UCSC Ensembl
Innerchr16:11631856..11661955hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3830100
hg1930100
hg1830100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150533
SamplesHGDP01211
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571457
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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