A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521606



Internal ID15448899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:90926645..90935157hg38UCSC Ensembl
Innerchr4:91847796..91856308hg19UCSC Ensembl
Innerchr4:92066819..92075331hg18UCSC Ensembl
Innerchr4:92204974..92213486hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg388513
hg198513
hg188513
hg178513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698223
Samples
Known GenesCCSER1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521606
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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