A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596311



Internal ID16383720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:182433286..182459799hg38UCSC Ensembl
Innerchr4:183354439..183380952hg19UCSC Ensembl
Innerchr4:183591433..183617946hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3826514
hg1926514
hg1826514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1017751
Samples
Known GenesTENM3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596311
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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