A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597730



Internal ID16385139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:28806149..28970066hg38UCSC Ensembl
Innerchr5:28806256..28970173hg19UCSC Ensembl
Innerchr5:28842013..29005930hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38163918
hg19163918
hg18163918
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9710n54
Supporting Variantsnssv1028726, nssv1028727
Samples
Known GenesLSP1P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597730
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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