A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586329



Internal ID16027052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:57525386..57526801hg38UCSC Ensembl
Innerchr20:56100442..56101857hg19UCSC Ensembl
Innerchr20:55533848..55535263hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg381416
hg191416
hg181416
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7619n54
Supporting Variantsnssv941754, nssv941757, nssv941756, nssv941755
Samples
Known GenesCTCFL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586329
Frequency
Sample Size17421
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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