A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528228



Internal ID15108835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:151905576..151943206hg38UCSC Ensembl
InnerchrX:151074048..151111678hg19UCSC Ensembl
InnerchrX:150824704..150862334hg18UCSC Ensembl
InnerchrX:150744616..150782246hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3837631
hg1937631
hg1837631
hg1737631
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704790
Samples
Known GenesMAGEA4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528228
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