A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046840



Internal ID19136059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:13325252..13348246hg38UCSC Ensembl
Innerchr16:13419109..13442103hg19UCSC Ensembl
Innerchr16:13326610..13349604hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3822995
hg1922995
hg1822995
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2737n100
Supporting Variantsnssv3557228, nssv3557229
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)nsv1046840
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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