A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065549



Internal ID18808080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:23943610..23995743hg38UCSC Ensembl
Innerchr22:24285797..24337937hg19UCSC Ensembl
Innerchr22:22615797..22667937hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3852134
hg1952141
hg1852141
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4534n100
Supporting Variantsnssv3586678, nssv3586679, nssv3586677
Samples
Known GenesDDT, DDTL, GSTT2, GSTT2B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065549
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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