A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065646



Internal ID18808177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14931037..14994037hg38UCSC Ensembl
Innerchr20:14911683..14974683hg19UCSC Ensembl
Innerchr20:14859683..14922683hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3863001
hg1963001
hg1863001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4275n100
Supporting Variantsnssv3599612
Samples
Known GenesMACROD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065646
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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