A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695187



Internal ID15085153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:26208070..27089369hg38UCSC Ensembl
InnerchrX:26226187..27107486hg19UCSC Ensembl
InnerchrX:26136108..27017407hg18UCSC Ensembl
InnerchrX:25985844..26867143hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38881300
hg19881300
hg18881300
hg17881300
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522405
Supporting Variants
Samples
Known GenesMAGEB5, VENTXP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695187
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