A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518680



Internal ID15445973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:30259856..30287751hg38UCSC Ensembl
InnerchrX:30277973..30305868hg19UCSC Ensembl
InnerchrX:30187894..30215789hg18UCSC Ensembl
InnerchrX:30037630..30065525hg17UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3827896
hg1927896
hg1827896
hg1727896
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696129
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518680
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