A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522306



Internal ID15102913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:27982484..28006636hg38UCSC Ensembl
Innerchr22:28378472..28402624hg19UCSC Ensembl
Innerchr22:26708472..26732624hg18UCSC Ensembl
Innerchr22:26703026..26727178hg17UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3824153
hg1924153
hg1824153
hg1724153
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694056
Samples
Known GenesMIR548AM, TTC28, TTC28-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522306
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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