A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059336



Internal ID18801867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:16384224..16804758hg38UCSC Ensembl
Innerchr22:16864886..17285648hg19UCSC Ensembl
Innerchr22:15244886..15665648hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38420535
hg19420763
hg18420763
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4459n100
Supporting Variantsnssv3589283
Samples
Known GenesANKRD62P1-PARP4P3, CCT8L2, TPTEP1, XKR3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059336
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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