A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522319



Internal ID15102926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:46615069..46628595hg38UCSC Ensembl
Innerchr1:47080741..47094267hg19UCSC Ensembl
Innerchr1:46853328..46866854hg18UCSC Ensembl
Innerchr1:46792761..46806287hg17UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3813527
hg1913527
hg1813527
hg1713527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695099
Samples
Known GenesMOB3C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522319
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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