A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3587392



Internal ID18538987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:21107944..21490766hg38UCSC Ensembl
Innerchr22:21462233..21845055hg19UCSC Ensembl
Innerchr22:19792233..20175055hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38382823
hg19382823
hg18382823
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056396
Supporting Variants
Samples
Known GenesBCRP2, FAM230B, HIC2, PI4KAP2, POM121L8P, RIMBP3B, RIMBP3C, TMEM191C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3587392
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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