A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521422



Internal ID15448715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:170887105..170903398hg38UCSC Ensembl
Innerchr4:171808256..171824549hg19UCSC Ensembl
Innerchr4:172044831..172061124hg18UCSC Ensembl
Innerchr4:172182986..172199279hg17UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3816294
hg1916294
hg1816294
hg1716294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698032
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521422
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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