A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058496



Internal ID19147715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:16577615..16594886hg38UCSC Ensembl
Innerchr20:16558260..16575531hg19UCSC Ensembl
Innerchr20:16506260..16523531hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3817272
hg1917272
hg1817272
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599641
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058496
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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