A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586322



Internal ID16027045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:57525340..57526763hg38UCSC Ensembl
Innerchr20:56100396..56101819hg19UCSC Ensembl
Innerchr20:55533802..55535225hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg381424
hg191424
hg181424
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7619n54
Supporting Variantsnssv941688, nssv941686, nssv941687, nssv941689
Samples
Known GenesCTCFL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586322
Frequency
Sample Size17421
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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