A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3003353



Internal ID16949619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:26772113..26773842hg38UCSC Ensembl
Outerchr22:27168076..27169805hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg381730
hg191730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv955463
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3003353
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer