A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516916



Internal ID15097523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:53465539..53475179hg38UCSC Ensembl
Innerchr4:54331706..54341346hg19UCSC Ensembl
Innerchr4:54026463..54036103hg18UCSC Ensembl
Innerchr4:54172634..54182274hg17UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg389641
hg199641
hg189641
hg179641
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv654968, nssv677157
Samples
Known GenesLNX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516916
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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