A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573660



Internal ID16014383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88572446..88573564hg38UCSC Ensembl
Innerchr16:88638854..88639972hg19UCSC Ensembl
Innerchr16:87166355..87167473hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg381119
hg191119
hg181119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5308n54
Supporting Variantsnssv863005
Samples
Known GenesZC3H18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573660
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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