A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586334



Internal ID16027057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:57525489..57526860hg38UCSC Ensembl
Innerchr20:56100545..56101916hg19UCSC Ensembl
Innerchr20:55533951..55535322hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg381372
hg191372
hg181372
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7619n54
Supporting Variantsnssv941765, nssv941764
Samples
Known GenesCTCFL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586334
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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