A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515664



Internal ID15443275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:19873352..19892114hg38UCSC Ensembl
Innerchr22:19860875..19879637hg19UCSC Ensembl
Innerchr22:18240875..18259637hg18UCSC Ensembl
Innerchr22:18235429..18254191hg17UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3818763
hg1918763
hg1818763
hg1718763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv659224, nssv664289, nssv690269, nssv665904, nssv670616
Samples
Known GenesTXNRD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515664
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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