A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061008



Internal ID18803539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:15351178..15922838hg38UCSC Ensembl
Innerchr22:16055171..16626785hg19UCSC Ensembl
Innerchr22:14435171..15006785hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38571661
hg19571615
hg18571615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589216
Samples
Known GenesBMS1P17, BMS1P18, OR11H1, POTEH
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061008
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