A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526137



Internal ID15453430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:21583386..21601629hg38UCSC Ensembl
Innerchr14:22051519..22069779hg19UCSC Ensembl
Innerchr14:21121359..21139619hg18UCSC Ensembl
Innerchr14:21121359..21139619hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3818244
hg1918261
hg1818261
hg1718261
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702392
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526137
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