A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589298



Internal ID18540893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:16384224..16807330hg38UCSC Ensembl
Innerchr22:16864886..17288220hg19UCSC Ensembl
Innerchr22:15244886..15668220hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38423107
hg19423335
hg18423335
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058669
Supporting Variants
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)nssv3589298
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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