A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586480



Internal ID16373889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62143364..62144394hg38UCSC Ensembl
Innerchr20:60718420..60719450hg19UCSC Ensembl
Innerchr20:60151815..60152845hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381031
hg191031
hg181031
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7648n54
Supporting Variantsnssv942093, nssv942088, nssv942102, nssv942109, nssv942090, nssv942086, nssv942099, nssv942100, nssv942082, nssv942097, nssv942108, nssv942091, nssv942092, nssv942089, nssv942104, nssv942101, nssv942111, nssv942098, nssv942087, nssv942080, nssv942103, nssv942081, nssv942095, nssv942106, nssv942084, nssv942083, nssv942094, nssv942096, nssv942110, nssv942107, nssv942085, nssv942105
Samples
Known GenesPSMA7, SS18L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586480
Frequency
Sample Size17421
Observed Gain29
Observed Loss3
Observed Complex0
Frequencyn/a


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