A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060264



Internal ID19149483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:16584517..16605899hg38UCSC Ensembl
Innerchr20:16565162..16586544hg19UCSC Ensembl
Innerchr20:16513162..16534544hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3821383
hg1921383
hg1821383
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4281n100
Supporting Variantsnssv3599644
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060264
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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