A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525519



Internal ID15452812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:98559306..98673534hg38UCSC Ensembl
InnerchrX:97814304..97928532hg19UCSC Ensembl
InnerchrX:97700960..97815188hg18UCSC Ensembl
InnerchrX:97620449..97734677hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38114229
hg19114229
hg18114229
hg17114229
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv521n21
Supporting Variantsnssv701652
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525519
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