A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3733082



Internal ID19031363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:22326560..22871175hg38UCSC Ensembl
Innerchr22:22680918..23213354hg19UCSC Ensembl
Innerchr22:21010918..21543354hg18UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg38544616
hg19532437
hg18532437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056723
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)nssv3733082
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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