A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519969



Internal ID15447262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:119494790..119503363hg38UCSC Ensembl
InnerchrX:118628753..118637326hg19UCSC Ensembl
InnerchrX:118512781..118521354hg18UCSC Ensembl
InnerchrX:118410635..118419208hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg388574
hg198574
hg188574
hg178574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697153
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519969
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer