A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518217



Internal ID15098824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:101118934..101120892hg38UCSC Ensembl
Innerchr4:102040091..102042049hg19UCSC Ensembl
Innerchr4:102259114..102261072hg18UCSC Ensembl
Innerchr4:102397269..102399227hg17UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg381959
hg191959
hg181959
hg171959
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695642
Samples
Known GenesPPP3CA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518217
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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