A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596453



Internal ID16037176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:187540004..188871837hg38UCSC Ensembl
Innerchr4:188461158..189792991hg19UCSC Ensembl
Innerchr4:188698152..190029985hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg381331834
hg191331834
hg181331834
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9441n54
Supporting Variantsnssv1020490
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)nsv596453
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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