A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520680



Internal ID15447973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:134001210..134274527hg38UCSC Ensembl
Innerchr4:134922365..135195682hg19UCSC Ensembl
Innerchr4:135141815..135415132hg18UCSC Ensembl
Innerchr4:135279970..135553287hg17UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38273318
hg19273318
hg18273318
hg17273318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv692757, nssv673952
Samples
Known GenesPABPC4L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520680
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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