A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060422



Internal ID19149641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86660704..86686888hg38UCSC Ensembl
Innerchr16:86694310..86720494hg19UCSC Ensembl
Innerchr16:85251811..85277995hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3826185
hg1926185
hg1826185
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559976
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)nsv1060422
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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