A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522288



Internal ID15449581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:40277914..40283721hg38UCSC Ensembl
Innerchr4:40279534..40285341hg19UCSC Ensembl
Innerchr4:39955929..39961736hg18UCSC Ensembl
Innerchr4:40102100..40107907hg17UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg385808
hg195808
hg185808
hg175808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695070
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522288
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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