A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062907



Internal ID18805438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14869207..14912974hg38UCSC Ensembl
Innerchr20:14849853..14893620hg19UCSC Ensembl
Innerchr20:14797853..14841620hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3843768
hg1943768
hg1843768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599595
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)nsv1062907
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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