A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063124



Internal ID19152343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1907315..1973548hg38UCSC Ensembl
Innerchr18:1907316..1973549hg19UCSC Ensembl
Innerchr18:1897316..1963549hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3866234
hg1966234
hg1866234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3311n100
Supporting Variantsnssv3725262
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)nsv1063124
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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