A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586321



Internal ID16027044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:57525185..57527189hg38UCSC Ensembl
Innerchr20:56100241..56102245hg19UCSC Ensembl
Innerchr20:55533647..55535651hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg382005
hg192005
hg182005
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7621n54
Supporting Variantsnssv941685, nssv941679, nssv941680, nssv941681, nssv941675, nssv941668, nssv941683, nssv941677, nssv941678, nssv941670, nssv941682, nssv941684, nssv941673, nssv941672, nssv941671, nssv941676, nssv941669, nssv941674
Samples
Known GenesCTCFL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586321
Frequency
Sample Size17421
Observed Gain16
Observed Loss2
Observed Complex0
Frequencyn/a


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