A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597027



Internal ID16384436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8015946..8020053hg38UCSC Ensembl
Innerchr5:8016059..8020166hg19UCSC Ensembl
Innerchr5:8069059..8073166hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg384108
hg194108
hg184108
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1023910
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597027
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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