A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062254



Internal ID19151473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:37601903..37659011hg38UCSC Ensembl
Innerchr18:35181866..35238974hg19UCSC Ensembl
Innerchr18:33435864..33492972hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3857109
hg1957109
hg1857109
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564210
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)nsv1062254
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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