A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061128



Internal ID19150347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59544227..59561218hg38UCSC Ensembl
Innerchr18:57211459..57228450hg19UCSC Ensembl
Innerchr18:55362439..55379430hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3816992
hg1916992
hg1816992
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3365n100
Supporting Variantsnssv3565494
Samples
Known GenesCCBE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061128
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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