A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526680



Internal ID15107287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103960706..104102135hg38UCSC Ensembl
Innerchr14:104427043..104568472hg19UCSC Ensembl
Innerchr14:103496796..103638225hg18UCSC Ensembl
Innerchr14:103496796..103638225hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38141430
hg19141430
hg18141430
hg17141430
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703012
Samples
Known GenesASPG, TDRD9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526680
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