A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061639



Internal ID18804170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:21960940..22225429hg38UCSC Ensembl
Innerchr22:22315312..22579822hg19UCSC Ensembl
Innerchr22:20645312..20909822hg18UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg38264490
hg19264511
hg18264511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4496n100
Supporting Variantsnssv3588868
Samples
Known GenesTOP3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061639
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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