A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586324



Internal ID16027047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:57525340..57526860hg38UCSC Ensembl
Innerchr20:56100396..56101916hg19UCSC Ensembl
Innerchr20:55533802..55535322hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg381521
hg191521
hg181521
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7619n54
Supporting Variantsnssv941706, nssv941707, nssv941712, nssv941704, nssv941713, nssv941709, nssv941710, nssv941711, nssv941705, nssv941715, nssv941702, nssv941714, nssv941701, nssv941703, nssv941708, nssv941716
Samples
Known GenesCTCFL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586324
Frequency
Sample Size17421
Observed Gain12
Observed Loss4
Observed Complex0
Frequencyn/a


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