A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057618



Internal ID19146837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:25684819..25764075hg38UCSC Ensembl
Innerchr20:25665455..25744711hg19UCSC Ensembl
Innerchr20:25613455..25692711hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3879257
hg1979257
hg1879257
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4291n100
Supporting Variantsnssv3737183
Samples
Known GenesFAM182B, ZNF337
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057618
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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