A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042556



Internal ID18785087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15886652..15923634hg38UCSC Ensembl
Innerchr16:15980509..16017491hg19UCSC Ensembl
Innerchr16:15888010..15924992hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3836983
hg1936983
hg1836983
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2773n100
Supporting Variantsnssv3557979, nssv3557977, nssv3557978
Samples
Known GenesFOPNL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042556
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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