A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060583



Internal ID19149802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1905345..1987525hg38UCSC Ensembl
Innerchr18:1905346..1987526hg19UCSC Ensembl
Innerchr18:1895346..1977526hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3882181
hg1982181
hg1882181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3311n100
Supporting Variantsnssv3564018, nssv3564019
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)nsv1060583
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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