A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519384



Internal ID15099991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:18924138..18931063hg38UCSC Ensembl
Innerchr9:18924136..18931061hg19UCSC Ensembl
Innerchr9:18914136..18921061hg18UCSC Ensembl
Innerchr9:18914136..18921061hg17UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg386926
hg196926
hg186926
hg176926
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv655768, nssv689027
Samples
Known GenesFAM154A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519384
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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