A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065954



Internal ID18808485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14826249..14915307hg38UCSC Ensembl
Innerchr20:14806895..14895953hg19UCSC Ensembl
Innerchr20:14754895..14843953hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3889059
hg1989059
hg1889059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4268n100
Supporting Variantsnssv3599578
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)nsv1065954
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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