A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571479



Internal ID16358888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12625942..12639410hg38UCSC Ensembl
Innerchr16:12719799..12733267hg19UCSC Ensembl
Innerchr16:12627300..12640768hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3813469
hg1913469
hg1813469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852544
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571479
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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