A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061088



Internal ID19150307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1183127..1461228hg38UCSC Ensembl
Innerchr18:1183128..1461229hg19UCSC Ensembl
Innerchr18:1173128..1451229hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38278102
hg19278102
hg18278102
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3309n100
Supporting Variantsnssv3563900
Samples
Known GenesLINC00470
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061088
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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