A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv949437



Internal ID15896707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:15479576..15885582hg38UCSC Ensembl
Innerchr22:16092381..16498387hg19UCSC Ensembl
Innerchr22:14472381..14878387hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38406007
hg19406007
hg18406007
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv588012
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, OR11H1, POTEH
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv949437
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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