A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151235



Internal ID15879860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14868013..14986860hg38UCSC Ensembl
Innerchr20:14848659..14967506hg19UCSC Ensembl
Innerchr20:14796659..14915506hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38118848
hg19118848
hg18118848
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585539
Supporting Variants
SamplesNINDS_117
Known GenesMACROD2, MACROD2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151235
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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