A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527279



Internal ID15107886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:86796784..87814130hg38UCSC Ensembl
Innerchr3:86845934..87863280hg19UCSC Ensembl
Innerchr3:86928624..87945970hg18UCSC Ensembl
Innerchr3:86928624..87945970hg17UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg381017347
hg191017347
hg181017347
hg171017347
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703691
Samples
Known GenesCHMP2B, LINC00506, MIR4795, POU1F1, VGLL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527279
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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