A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525367



Internal ID15452660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48631572..48760764hg38UCSC Ensembl
Innerchr14:49100775..49229967hg19UCSC Ensembl
Innerchr14:48170525..48299717hg18UCSC Ensembl
Innerchr14:48170525..48299717hg17UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38129193
hg19129193
hg18129193
hg17129193
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701487
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525367
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