A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594008



Internal ID16034731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:38664272..38665235hg38UCSC Ensembl
Innerchr4:38665893..38666856hg19UCSC Ensembl
Innerchr4:38342288..38343251hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38964
hg19964
hg18964
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9015n54
Supporting Variantsnssv995928, nssv995927
Samples
Known GenesFLJ13197, KLF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594008
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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