A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573366



Internal ID16360775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82102961..82164278hg38UCSC Ensembl
Innerchr16:82136566..82197883hg19UCSC Ensembl
Innerchr16:80694067..80755384hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3861318
hg1961318
hg1861318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5251n54
Supporting Variantsnssv861942
Samples
Known GenesMPHOSPH6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573366
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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