A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066105



Internal ID19155324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14221263..14291469hg38UCSC Ensembl
Innerchr20:14201909..14272115hg19UCSC Ensembl
Innerchr20:14149909..14220115hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3870207
hg1970207
hg1870207
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3734878
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)nsv1066105
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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