A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573820



Internal ID16361229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89907493..89908339hg38UCSC Ensembl
Innerchr16:89973901..89974747hg19UCSC Ensembl
Innerchr16:88501402..88502248hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38847
hg19847
hg18847
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5336n54
Supporting Variantsnssv863743, nssv863741, nssv863738, nssv863739, nssv863737, nssv863742, nssv863740
Samples
Known GenesTCF25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573820
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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