A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573586



Internal ID16014309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88415706..88485962hg38UCSC Ensembl
Innerchr16:88482114..88552370hg19UCSC Ensembl
Innerchr16:87009615..87079871hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3870257
hg1970257
hg1870257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5293n54
Supporting Variantsnssv862558
Samples
Known GenesMIR5189, ZFPM1, ZNF469
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573586
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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