A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv957294



Internal ID16251250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:48899333..48970311hg38UCSC Ensembl
Innerchr22:49295145..49366123hg19UCSC Ensembl
Innerchr22:47681149..47752127hg18UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg3870979
hg1970979
hg1870979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589168
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv957294
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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