A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521825



Internal ID15449118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:32492585..32526438hg38UCSC Ensembl
InnerchrX:32510702..32544555hg19UCSC Ensembl
InnerchrX:32420623..32454476hg18UCSC Ensembl
InnerchrX:32270359..32304212hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3833854
hg1933854
hg1833854
hg1733854
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694598
Samples
Known GenesDMD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521825
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