A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597714



Internal ID16385123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:28763545..28874006hg38UCSC Ensembl
Innerchr5:28763652..28874113hg19UCSC Ensembl
Innerchr5:28799409..28909870hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38110462
hg19110462
hg18110462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9706n54
Supporting Variantsnssv1153298
SamplesHGDP00923
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597714
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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