A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573290



Internal ID16360699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79819370..79905607hg38UCSC Ensembl
Innerchr16:79853267..79939504hg19UCSC Ensembl
Innerchr16:78410768..78497005hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3886238
hg1986238
hg1886238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv861696
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573290
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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