A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573823



Internal ID16361232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89907493..89908507hg38UCSC Ensembl
Innerchr16:89973901..89974915hg19UCSC Ensembl
Innerchr16:88501402..88502416hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381015
hg191015
hg181015
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5337n54
Supporting Variantsnssv863759, nssv863756, nssv863760, nssv863757, nssv863755, nssv863762, nssv863758, nssv863761, nssv863754
Samples
Known GenesTCF25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573823
Frequency
Sample Size17421
Observed Gain7
Observed Loss2
Observed Complex0
Frequencyn/a


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