A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528113



Internal ID8422388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:150061081..150064584hg38UCSC Ensembl
Innerchr5:149440644..149444147hg19UCSC Ensembl
Innerchr5:149420837..149424340hg18UCSC Ensembl
Innerchr5:149420837..149424340hg17UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg383504
hg193504
hg183504
hg173504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704655
Samples
Known GenesCSF1R
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528113
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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