A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596455



Internal ID16383864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:187776941..188300053hg38UCSC Ensembl
Innerchr4:188698095..189221207hg19UCSC Ensembl
Innerchr4:188935089..189458201hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38523113
hg19523113
hg18523113
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9442n54
Supporting Variantsnssv1152852
SamplesHGDP01033
Known GenesTRIML1, TRIML2, ZFP42
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596455
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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