A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597167



Internal ID16384576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:12765180..12882940hg38UCSC Ensembl
Innerchr5:12765292..12883052hg19UCSC Ensembl
Innerchr5:12818292..12936052hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38117761
hg19117761
hg18117761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9586n54
Supporting Variantsnssv1025310
Samples
Known GenesCT49
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597167
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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