A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059826



Internal ID18802357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:77564504..78799796hg38UCSC Ensembl
Innerchr18:75276460..76559796hg19UCSC Ensembl
Innerchr18:73405448..74660784hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381235293
hg191283337
hg181255337
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3407n100
Supporting Variantsnssv3563043
Samples
Known GenesLINC01029
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059826
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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