A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526028



Internal ID15453321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:47379973..47380714hg38UCSC Ensembl
Innerchr6:47347709..47348450hg19UCSC Ensembl
Innerchr6:47455668..47456409hg18UCSC Ensembl
Innerchr6:47455668..47456409hg17UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38742
hg19742
hg18742
hg17742
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702259
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526028
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