A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520911



Internal ID15448204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:107742077..107755513hg38UCSC Ensembl
Innerchr9:110504358..110517794hg19UCSC Ensembl
Innerchr9:109544179..109557615hg18UCSC Ensembl
Innerchr9:107583913..107597349hg17UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3813437
hg1913437
hg1813437
hg1713437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv679368, nssv677564
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520911
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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