A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063855



Internal ID18806386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:25057433..25126693hg38UCSC Ensembl
Innerchr16:25068754..25138014hg19UCSC Ensembl
Innerchr16:24976255..25045515hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3869261
hg1969261
hg1869261
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2827n100
Supporting Variantsnssv3549131
Samples
Known GenesLCMT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063855
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