A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594004



Internal ID16381413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:38663996..38665125hg38UCSC Ensembl
Innerchr4:38665617..38666746hg19UCSC Ensembl
Innerchr4:38342012..38343141hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381130
hg191130
hg181130
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9014n54
Supporting Variantsnssv995923
Samples
Known GenesFLJ13197, KLF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594004
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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