A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv862568



Internal ID15809838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88533472..88539757hg38UCSC Ensembl
Innerchr16:88599880..88606165hg19UCSC Ensembl
Innerchr16:87127381..87133666hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg386286
hg196286
hg186286
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573593
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)nssv862568
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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