A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059093



Internal ID19148312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76996818..77015675hg38UCSC Ensembl
Innerchr18:74708774..74727631hg19UCSC Ensembl
Innerchr18:72837762..72856619hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3818858
hg1918858
hg1818858
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3563041
Samples
Known GenesMBP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059093
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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