A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3725298



Internal ID19023579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:22405498..22430278hg38UCSC Ensembl
Innerchr18:19985461..20010241hg19UCSC Ensembl
Innerchr18:18239459..18264239hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3824781
hg1924781
hg1824781
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063934
Supporting Variants
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)nssv3725298
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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