A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517803



Internal ID15098410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:39859533..39991467hg38UCSC Ensembl
Innerchr3:39901024..40032958hg19UCSC Ensembl
Innerchr3:39876028..40007962hg18UCSC Ensembl
Innerchr3:39876028..40007962hg17UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38131935
hg19131935
hg18131935
hg17131935
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695207
Samples
Known GenesMYRIP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517803
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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