A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573786



Internal ID16014509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89830570..89831943hg38UCSC Ensembl
Innerchr16:89896978..89898351hg19UCSC Ensembl
Innerchr16:88424479..88425852hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381374
hg191374
hg181374
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5329n54
Supporting Variantsnssv863575, nssv863576, nssv863574
Samples
Known GenesSPIRE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573786
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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