A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597720



Internal ID16385129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:28792606..28874006hg38UCSC Ensembl
Innerchr5:28792713..28874113hg19UCSC Ensembl
Innerchr5:28828470..28909870hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3881401
hg1981401
hg1881401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9706n54
Supporting Variantsnssv1153301
SamplesHGDP00933
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597720
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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