A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573590



Internal ID16014313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88533472..88533592hg38UCSC Ensembl
Innerchr16:88599880..88600000hg19UCSC Ensembl
Innerchr16:87127381..87127501hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38121
hg19121
hg18121
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv862562
Samples
Known GenesZFPM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573590
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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