A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597143



Internal ID16384552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:10760959..10761497hg38UCSC Ensembl
Innerchr5:10761071..10761609hg19UCSC Ensembl
Innerchr5:10814071..10814609hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38539
hg19539
hg18539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1025285
Samples
Known GenesDAP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597143
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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