A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522266



Internal ID15102873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:31484040..31536428hg38UCSC Ensembl
InnerchrX:31502157..31554545hg19UCSC Ensembl
InnerchrX:31412078..31464466hg18UCSC Ensembl
InnerchrX:31261814..31314202hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3852389
hg1952389
hg1852389
hg1752389
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695046
Samples
Known GenesDMD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522266
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