A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv599718



Internal ID16387127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:133403634..133415480hg38UCSC Ensembl
Innerchr5:132739326..132751172hg19UCSC Ensembl
Innerchr5:132767225..132779071hg18UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3811847
hg1911847
hg1811847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1032516
Samples
Known GenesFSTL4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv599718
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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