A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066486



Internal ID19155705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:31973728..32002015hg38UCSC Ensembl
Innerchr18:29553691..29581978hg19UCSC Ensembl
Innerchr18:27807689..27835976hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3828288
hg1928288
hg1828288
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3329n100
Supporting Variantsnssv3564166
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)nsv1066486
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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