A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573343



Internal ID16360752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81035693..81036454hg38UCSC Ensembl
Innerchr16:81069298..81070059hg19UCSC Ensembl
Innerchr16:79626799..79627560hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38762
hg19762
hg18762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5247n54
Supporting Variantsnssv861924
Samples
Known GenesATMIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573343
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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