A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573533



Internal ID16360942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87550707..87589874hg38UCSC Ensembl
Innerchr16:87584313..87623480hg19UCSC Ensembl
Innerchr16:86141814..86180981hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3839168
hg1939168
hg1839168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150559
SamplesHGDP00607
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573533
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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