A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586258



Internal ID16026981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54031291..54041462hg38UCSC Ensembl
Innerchr20:52647830..52658001hg19UCSC Ensembl
Innerchr20:52081237..52091408hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3810172
hg1910172
hg1810172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7608n54
Supporting Variantsnssv941503, nssv941496, nssv941499, nssv941504, nssv941502, nssv941505, nssv941501, nssv941498, nssv941497, nssv941500
Samples
Known GenesBCAS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586258
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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