A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061451



Internal ID19150670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:22402491..22427689hg38UCSC Ensembl
Innerchr18:19982454..20007652hg19UCSC Ensembl
Innerchr18:18236452..18261650hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3825199
hg1925199
hg1825199
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3325n100
Supporting Variantsnssv3564130
Samples
Known GenesCTAGE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061451
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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