A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059509



Internal ID18802040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:11543..190140hg38UCSC Ensembl
Innerchr18:11543..190140hg19UCSC Ensembl
Innerchr18:1543..180140hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38178598
hg19178598
hg18178598
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3300n100
Supporting Variantsnssv3569022
Samples
Known GenesMIR8078, ROCK1P1, USP14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059509
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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