A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573825



Internal ID16014548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89907493..89909816hg38UCSC Ensembl
Innerchr16:89973901..89976224hg19UCSC Ensembl
Innerchr16:88501402..88503725hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg382324
hg192324
hg182324
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv863980, nssv863978, nssv863979, nssv863982, nssv863981
Samples
Known GenesTCF25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573825
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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