A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066888



Internal ID18809419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:79643023..79769924hg38UCSC Ensembl
Innerchr18:77403023..77529924hg19UCSC Ensembl
Innerchr18:75504011..75630912hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38126902
hg19126902
hg18126902
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3563064
Samples
Known GenesCTDP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066888
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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