A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058492



Internal ID19147711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:9995048..10115536hg38UCSC Ensembl
Innerchr18:9995045..10115533hg19UCSC Ensembl
Innerchr18:9985045..10105533hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38120489
hg19120489
hg18120489
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3320n100
Supporting Variantsnssv3725290
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)nsv1058492
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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