A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596456



Internal ID16037179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:187865684..188095782hg38UCSC Ensembl
Innerchr4:188786838..189016936hg19UCSC Ensembl
Innerchr4:189023832..189253930hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38230099
hg19230099
hg18230099
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152853
SamplesHGDP00734
Known GenesTRIML2, ZFP42
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596456
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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