A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599413



Internal ID18551008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14653006..14906724hg38UCSC Ensembl
Innerchr20:14633652..14887370hg19UCSC Ensembl
Innerchr20:14581652..14835370hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38253719
hg19253719
hg18253719
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062048
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)nssv3599413
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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