A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066670



Internal ID19155889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59615985..59642465hg38UCSC Ensembl
Innerchr18:57283217..57309697hg19UCSC Ensembl
Innerchr18:55434197..55460677hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3826481
hg1926481
hg1826481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565495
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)nsv1066670
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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