A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv862588



Internal ID15809858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88533696..88547771hg38UCSC Ensembl
Innerchr16:88600104..88614179hg19UCSC Ensembl
Innerchr16:87127605..87141680hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3814076
hg1914076
hg1814076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573606
Supporting Variants
Samples
Known GenesZFPM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv862588
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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