A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067554



Internal ID18810085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:21960940..22027424hg38UCSC Ensembl
Innerchr22:22315312..22381822hg19UCSC Ensembl
Innerchr22:20645312..20711822hg18UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg3866485
hg1966511
hg1866511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3588864
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)nsv1067554
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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