A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062166



Internal ID18804697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:36843747..36872271hg38UCSC Ensembl
Innerchr18:34423710..34452234hg19UCSC Ensembl
Innerchr18:32677708..32706232hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3828525
hg1928525
hg1828525
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564204
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)nsv1062166
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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