A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3588864



Internal ID18540459
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 StatusS
Merged Variantsnsv1067554
Supporting Variants
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)nssv3588864
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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