A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055503



Internal ID18798034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84577279..84613367hg38UCSC Ensembl
Innerchr16:84610885..84646973hg19UCSC Ensembl
Innerchr16:83168386..83204474hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3836089
hg1936089
hg1836089
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559958
Samples
Known GenesCOTL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055503
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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