A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058887



Internal ID19148106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14099468..14192888hg38UCSC Ensembl
Innerchr20:14080114..14173534hg19UCSC Ensembl
Innerchr20:14028114..14121534hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3893421
hg1993421
hg1893421
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3734877
Samples
Known GenesMACROD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058887
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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