A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058706



Internal ID19147925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:74395163..74420068hg38UCSC Ensembl
Innerchr18:72062398..72087303hg19UCSC Ensembl
Innerchr18:70213378..70238283hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3824906
hg1924906
hg1824906
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3403n100
Supporting Variantsnssv3563018
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)nsv1058706
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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