A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066060



Internal ID19155279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:38312380..38418879hg38UCSC Ensembl
Innerchr18:35892344..35998843hg19UCSC Ensembl
Innerchr18:34146342..34252841hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38106500
hg19106500
hg18106500
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3725317
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)nsv1066060
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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