A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588872



Internal ID16029595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:27131043..27785448hg38UCSC Ensembl
Innerchr22:27527005..28181436hg19UCSC Ensembl
Innerchr22:25857005..26511436hg18UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38654406
hg19654432
hg18654432
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv954550
Samples
Known GenesMN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588872
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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