A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067561



Internal ID19156780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14863403..14887707hg38UCSC Ensembl
Innerchr20:14844049..14868353hg19UCSC Ensembl
Innerchr20:14792049..14816353hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3824305
hg1924305
hg1824305
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599594
Samples
Known GenesMACROD2, MACROD2-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067561
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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