A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1660049



Internal ID15495393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:20534818..20545787hg38UCSC Ensembl
Innerchr16:20546140..20557109hg19UCSC Ensembl
Innerchr16:20453641..20464610hg18UCSC Ensembl
Innerchr16:20453641..20464610hg17UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3810970
hg1910970
hg1810970
hg1710970
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv442394
Supporting Variants
SamplesNA19154
Known GenesACSM2B
MethodSNP array
AnalysisWe used two computational approaches to identify CNVs: the hidden Markov model Birdseye, and an approach based on correlation between nearby probes across a population sample. To maximize the quality of reported findings, we ran duplicate experiments in independent labs, and report the CNVs that were observed in both experiments, in the same samples and at essentially identical genomic locations.
Platform[GenomeWideSNP_6] Affymetrix Genome-Wide Human SNP 6.0 Array
Comments
ReferenceMcCarroll_et_al_2008
Pubmed ID18776908
Accession Number(s)nssv1660049
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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