A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528025



Internal ID15108632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:99778104..99851390hg38UCSC Ensembl
Innerchr9:102540386..102613672hg19UCSC Ensembl
Innerchr9:101580207..101653493hg18UCSC Ensembl
Innerchr9:99619941..99693227hg17UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3873287
hg1973287
hg1873287
hg1773287
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704554
Samples
Known GenesNR4A3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528025
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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