A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062378



Internal ID18804909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89073897..89168041hg38UCSC Ensembl
Innerchr16:89140305..89234449hg19UCSC Ensembl
Innerchr16:87667806..87761950hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3894145
hg1994145
hg1894145
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560002
Samples
Known GenesACSF3, LINC00304, LOC400558
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062378
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer