A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056797



Internal ID18799328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14834988..14960926hg38UCSC Ensembl
Innerchr20:14815634..14941572hg19UCSC Ensembl
Innerchr20:14763634..14889572hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38125939
hg19125939
hg18125939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599584
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)nsv1056797
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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