A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520336



Internal ID15447629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:51295971..51298854hg38UCSC Ensembl
Innerchr14:51762689..51765572hg19UCSC Ensembl
Innerchr14:50832439..50835322hg18UCSC Ensembl
Innerchr14:50832439..50835322hg17UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg382884
hg192884
hg182884
hg172884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697355
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520336
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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