A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519266



Internal ID15099873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:107287196..107322974hg38UCSC Ensembl
Innerchr9:110049477..110085255hg19UCSC Ensembl
Innerchr9:109089298..109125076hg18UCSC Ensembl
Innerchr9:107129032..107164810hg17UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3835779
hg1935779
hg1835779
hg1735779
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696756
Samples
Known GenesRAD23B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519266
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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