A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3586510



Internal ID18538105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:23255083..23630873hg38UCSC Ensembl
Innerchr22:23597270..23973060hg19UCSC Ensembl
Innerchr22:21927270..22303060hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38375791
hg19375791
hg18375791
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059951
Supporting Variants
Samples
Known GenesBCR, C22orf43, CES5AP1, FBXW4P1, IGLL1, ZDHHC8P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3586510
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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