A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3733098



Internal ID19031379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:22385940..22881053hg38UCSC Ensembl
Innerchr22:22740307..23223233hg19UCSC Ensembl
Innerchr22:21070307..21553233hg18UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg38495114
hg19482927
hg18482927
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066349
Supporting Variants
Samples
Known GenesGGTLC2, LOC648691, MIR650, POM121L1P, PRAME, ZNF280A, ZNF280B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3733098
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