A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586271



Internal ID16026994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54036316..54041462hg38UCSC Ensembl
Innerchr20:52652855..52658001hg19UCSC Ensembl
Innerchr20:52086262..52091408hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg385147
hg195147
hg185147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7611n54
Supporting Variantsnssv941554, nssv941547, nssv941549, nssv941546, nssv941550, nssv941551, nssv941548, nssv941552, nssv941553
Samples
Known GenesBCAS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586271
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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