A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517359



Internal ID15444652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101378772..101393317hg38UCSC Ensembl
Innerchr14:101845109..101859654hg19UCSC Ensembl
Innerchr14:100914862..100929407hg18UCSC Ensembl
Innerchr14:100914862..100929407hg17UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3814546
hg1914546
hg1814546
hg1714546
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv651811, nssv668665, nssv677916, nssv696515, nssv701378, nssv679492
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517359
Frequency
Sample Size2026
Observed Gain5
Observed Loss1
Observed Complex0
Frequencyn/a


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