A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523125



Internal ID8417400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:150104198..150106209hg38UCSC Ensembl
Innerchr5:149483761..149485772hg19UCSC Ensembl
Innerchr5:149463954..149465965hg18UCSC Ensembl
Innerchr5:149463954..149465965hg17UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg382012
hg192012
hg182012
hg172012
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698827
Samples
Known GenesCSF1R
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523125
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