A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573821



Internal ID16361230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89907493..89908396hg38UCSC Ensembl
Innerchr16:89973901..89974804hg19UCSC Ensembl
Innerchr16:88501402..88502305hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38904
hg19904
hg18904
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5337n54
Supporting Variantsnssv863747, nssv863746, nssv863748, nssv863749, nssv863744, nssv863750, nssv863745
Samples
Known GenesTCF25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573821
Frequency
Sample Size17421
Observed Gain6
Observed Loss1
Observed Complex0
Frequencyn/a


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