A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704655



Internal ID15094621
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528113
Supporting Variants
Samples
Known GenesCSF1R
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704655
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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