A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060384



Internal ID18802915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:30791094..30867517hg38UCSC Ensembl
Innerchr16:30802415..30878838hg19UCSC Ensembl
Innerchr16:30709916..30786339hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3876424
hg1976424
hg1876424
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3549158
Samples
Known GenesBCL7C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060384
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