A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061983



Internal ID19151202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:74398731..74419015hg38UCSC Ensembl
Innerchr18:72065966..72086250hg19UCSC Ensembl
Innerchr18:70216946..70237230hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3820285
hg1920285
hg1820285
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3404n100
Supporting Variantsnssv3563021
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)nsv1061983
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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