A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064506



Internal ID18807037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:79580427..79773771hg38UCSC Ensembl
Innerchr18:77340427..77533771hg19UCSC Ensembl
Innerchr18:75441415..75634759hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38193345
hg19193345
hg18193345
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3563063
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)nsv1064506
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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