A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600279



Internal ID16041002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:171448172..171493699hg38UCSC Ensembl
Innerchr5:170875176..170920703hg19UCSC Ensembl
Innerchr5:170807781..170853308hg18UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3845528
hg1945528
hg1845528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1045478
Samples
Known GenesFGF18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600279
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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