A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522702



Internal ID15449995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:51295971..51327698hg38UCSC Ensembl
Innerchr14:51762689..51794416hg19UCSC Ensembl
Innerchr14:50832439..50864166hg18UCSC Ensembl
Innerchr14:50832439..50864166hg17UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3831728
hg1931728
hg1831728
hg1731728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706113
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522702
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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