A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520837



Internal ID15448130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:86669193..86689587hg38UCSC Ensembl
InnerchrX:85924196..85944590hg19UCSC Ensembl
InnerchrX:85810852..85831246hg18UCSC Ensembl
InnerchrX:85730341..85750735hg17UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg3820395
hg1920395
hg1820395
hg1720395
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697642
Samples
Known GenesDACH2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520837
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