A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv599395



Internal ID16386804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:113034614..113093172hg38UCSC Ensembl
Innerchr5:112370311..112428869hg19UCSC Ensembl
Innerchr5:112398210..112456768hg18UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg3858559
hg1958559
hg1858559
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1040382
Samples
Known GenesMCC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv599395
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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