A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059538



Internal ID19148757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:70811095..70866704hg38UCSC Ensembl
Innerchr18:68478331..68533940hg19UCSC Ensembl
Innerchr18:66629311..66684920hg18UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg3855610
hg1955610
hg1855610
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3723220
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)nsv1059538
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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