A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596622



Internal ID16037345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:361582..393262hg38UCSC Ensembl
Innerchr5:361697..393377hg19UCSC Ensembl
Innerchr5:414697..446377hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3831681
hg1931681
hg1831681
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1021067
Samples
Known GenesAHRR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596622
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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