A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589341



Internal ID18540936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:17883901..17965363hg38UCSC Ensembl
Innerchr22:18366667..18448129hg19UCSC Ensembl
Innerchr22:16746667..16828129hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3881463
hg1981463
hg1881463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065486
Supporting Variants
Samples
Known GenesMICAL3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3589341
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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