A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573668



Internal ID16014391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88572446..88577049hg38UCSC Ensembl
Innerchr16:88638854..88643457hg19UCSC Ensembl
Innerchr16:87166355..87170958hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg384604
hg194604
hg184604
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv863075
Samples
Known GenesZC3H18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573668
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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