A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055803



Internal ID18798334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14786706..14888657hg38UCSC Ensembl
Innerchr20:14767352..14869303hg19UCSC Ensembl
Innerchr20:14715352..14817303hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38101952
hg19101952
hg18101952
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599461
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)nsv1055803
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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