A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521429



Internal ID15448722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:128601345..128605106hg38UCSC Ensembl
Innerchr11:128471240..128475001hg19UCSC Ensembl
Innerchr11:127976450..127980211hg18UCSC Ensembl
Innerchr11:127976450..127980211hg17UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg383762
hg193762
hg183762
hg173762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698039
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521429
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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