A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596452



Internal ID16037175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:187540004..188752130hg38UCSC Ensembl
Innerchr4:188461158..189673284hg19UCSC Ensembl
Innerchr4:188698152..189910278hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg381212127
hg191212127
hg181212127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9441n54
Supporting Variantsnssv1020489
Samples
Known GenesLINC01060, TRIML1, TRIML2, ZFP42
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596452
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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