A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060372



Internal ID18802903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:53792469..53885561hg38UCSC Ensembl
Innerchr20:52409008..52502100hg19UCSC Ensembl
Innerchr20:51842415..51935507hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3893093
hg1993093
hg1893093
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3731369
Samples
Known GenesSUMO1P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060372
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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