A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586119



Internal ID16026842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45714903..45749420hg38UCSC Ensembl
Innerchr20:44343542..44378059hg19UCSC Ensembl
Innerchr20:43776956..43811466hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3834518
hg1934518
hg1834511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7590n54
Supporting Variantsnssv940839
Samples
Known GenesSPINT4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586119
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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