A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598643



Internal ID16039366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:73445575..73447987hg38UCSC Ensembl
Innerchr5:72741402..72743812hg19UCSC Ensembl
Innerchr5:72777158..72779568hg18UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg382413
hg192411
hg182411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1035082
Samples
Known GenesFOXD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598643
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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