A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573666



Internal ID16014389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88572446..88575580hg38UCSC Ensembl
Innerchr16:88638854..88641988hg19UCSC Ensembl
Innerchr16:87166355..87169489hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg383135
hg193135
hg183135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5309n54
Supporting Variantsnssv863019, nssv863020, nssv863021, nssv863018
Samples
Known GenesZC3H18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573666
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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