A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059531



Internal ID18802062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38124868..38169202hg38UCSC Ensembl
Innerchr22:38520875..38565209hg19UCSC Ensembl
Innerchr22:36850821..36895155hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3844335
hg1944335
hg1844335
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600877
Samples
Known GenesPLA2G6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059531
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