A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524475



Internal ID15451768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:99920247..99954659hg38UCSC Ensembl
Innerchr14:100386584..100420996hg19UCSC Ensembl
Innerchr14:99456337..99490749hg18UCSC Ensembl
Innerchr14:99456337..99490749hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3834413
hg1934413
hg1834413
hg1734413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700413
Samples
Known GenesEML1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524475
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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