A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066589



Internal ID18809120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:36835846..36853023hg38UCSC Ensembl
Innerchr18:34415809..34432986hg19UCSC Ensembl
Innerchr18:32669807..32686984hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3817178
hg1917178
hg1817178
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3335n100
Supporting Variantsnssv3564201
Samples
Known GenesKIAA1328
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066589
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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