A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599608



Internal ID18551203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14909985..15064766hg38UCSC Ensembl
Innerchr20:14890631..15045412hg19UCSC Ensembl
Innerchr20:14838631..14993412hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38154782
hg19154782
hg18154782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059656
Supporting Variants
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)nssv3599608
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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