A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528188



Internal ID15108795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:150061081..150070569hg38UCSC Ensembl
Innerchr5:149440644..149450132hg19UCSC Ensembl
Innerchr5:149420837..149430325hg18UCSC Ensembl
Innerchr5:149420837..149430325hg17UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg389489
hg199489
hg189489
hg179489
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704744
Samples
Known GenesCSF1R
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528188
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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