A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522821



Internal ID15450114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:144180232..144183185hg38UCSC Ensembl
Innerchr3:143899074..143902027hg19UCSC Ensembl
Innerchr3:145381764..145384717hg18UCSC Ensembl
Innerchr3:145381772..145384725hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg382954
hg192954
hg182954
hg172954
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698470
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522821
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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