A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062524



Internal ID18805055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:20044066..20066031hg38UCSC Ensembl
Innerchr22:20031589..20053554hg19UCSC Ensembl
Innerchr22:18411589..18433554hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3821966
hg1921966
hg1821966
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4479n100
Supporting Variantsnssv3587352
Samples
Known GenesTANGO2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062524
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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