A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518062



Internal ID15098669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:14571240..14611268hg38UCSC Ensembl
InnerchrX:14589362..14629390hg19UCSC Ensembl
InnerchrX:14499283..14539311hg18UCSC Ensembl
InnerchrX:14349019..14389047hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3840029
hg1940029
hg1840029
hg1740029
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695474
Samples
Known GenesGLRA2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518062
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