A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520455



Internal ID15447748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:57916119..57979157hg38UCSC Ensembl
InnerchrX:57942553..58005591hg19UCSC Ensembl
InnerchrX:57959278..58022316hg18UCSC Ensembl
InnerchrX:57825574..57888612hg17UCSC Ensembl
CytobandXp11.1
Allele length
AssemblyAllele length
hg3863039
hg1963039
hg1863039
hg1763039
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv671990, nssv671620
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520455
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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