A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056828



Internal ID19146047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:37632059..37663134hg38UCSC Ensembl
Innerchr18:35212022..35243097hg19UCSC Ensembl
Innerchr18:33466020..33497095hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3831076
hg1931076
hg1831076
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564211
Samples
Known GenesMIR4318
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056828
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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