A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060896



Internal ID18803427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33302560..33333777hg38UCSC Ensembl
Innerchr22:33698546..33729763hg19UCSC Ensembl
Innerchr22:32028546..32059763hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3831218
hg1931218
hg1831218
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600826
Samples
Known GenesLARGE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060896
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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