A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3592287



Internal ID18890568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:48759275..48779197hg38UCSC Ensembl
Innerchr22:49155087..49175009hg19UCSC Ensembl
Innerchr22:47541093..47561015hg18UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg3819923
hg1919923
hg1819923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056474
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3592287
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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