A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067363



Internal ID19156582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59986256..59996331hg38UCSC Ensembl
Innerchr18:57653488..57663563hg19UCSC Ensembl
Innerchr18:55804468..55814543hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3810076
hg1910076
hg1810076
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3368n100
Supporting Variantsnssv3565551, nssv3565554, nssv3565556, nssv3565555, nssv3565553, nssv3565552, nssv3565550
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)nsv1067363
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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