A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060415



Internal ID19149634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:44444542..44465096hg38UCSC Ensembl
Innerchr18:42024507..42045061hg19UCSC Ensembl
Innerchr18:40278505..40299059hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3820555
hg1920555
hg1820555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565370
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060415
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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