A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055223



Internal ID19144442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:47593465..47626454hg38UCSC Ensembl
Innerchr22:47989214..48022203hg19UCSC Ensembl
Innerchr22:46367878..46400867hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3832990
hg1932990
hg1832990
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3592274
Samples
Known GenesLINC00898
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055223
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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