A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516666



Internal ID15443959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:141209711..141231139hg38UCSC Ensembl
Innerchr8:142219810..142241238hg19UCSC Ensembl
Innerchr8:142288992..142310420hg18UCSC Ensembl
Innerchr8:142288992..142310420hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3821429
hg1921429
hg1821429
hg1721429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv656371, nssv671883, nssv670018, nssv693448
Samples
Known GenesSLC45A4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516666
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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