A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597928



Internal ID16385337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:43556492..43557043hg38UCSC Ensembl
Innerchr5:43556594..43557145hg19UCSC Ensembl
Innerchr5:43592351..43592902hg18UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38552
hg19552
hg18552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9738n54
Supporting Variantsnssv1029368
Samples
Known GenesPAIP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597928
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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