A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573604



Internal ID16014327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88533696..88534569hg38UCSC Ensembl
Innerchr16:88600104..88600977hg19UCSC Ensembl
Innerchr16:87127605..87128478hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38874
hg19874
hg18874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5297n54
Supporting Variantsnssv862586
Samples
Known GenesZFPM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573604
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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