A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062442



Internal ID19151661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:25733374..25774202hg38UCSC Ensembl
Innerchr20:25714010..25754838hg19UCSC Ensembl
Innerchr20:25662010..25702838hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3840829
hg1940829
hg1840829
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584682
Samples
Known GenesFAM182B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062442
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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