A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525973



Internal ID15453266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:4800596..4907452hg38UCSC Ensembl
InnerchrX:4718637..4825493hg19UCSC Ensembl
InnerchrX:4728637..4835493hg18UCSC Ensembl
InnerchrX:4578373..4685229hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg38106857
hg19106857
hg18106857
hg17106857
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv498n21
Supporting Variantsnssv702189
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525973
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