A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589281



Internal ID18540876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:16384224..16758662hg38UCSC Ensembl
Innerchr22:16864886..17239552hg19UCSC Ensembl
Innerchr22:15244886..15619552hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38374439
hg19374667
hg18374667
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056300
Supporting Variants
Samples
Known GenesANKRD62P1-PARP4P3, CCT8L2, TPTEP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3589281
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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