A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522452



Internal ID15449745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:169053605..169087796hg38UCSC Ensembl
Innerchr4:169974756..170008947hg19UCSC Ensembl
Innerchr4:170211331..170245522hg18UCSC Ensembl
Innerchr4:170349486..170383677hg17UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3834192
hg1934192
hg1834192
hg1734192
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705815
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522452
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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