A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573818



Internal ID16014541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89907493..89908228hg38UCSC Ensembl
Innerchr16:89973901..89974636hg19UCSC Ensembl
Innerchr16:88501402..88502137hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38736
hg19736
hg18736
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5338n54
Supporting Variantsnssv863724, nssv863720, nssv863719, nssv863725, nssv863721, nssv863722, nssv863723
Samples
Known GenesTCF25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573818
Frequency
Sample Size17421
Observed Gain5
Observed Loss2
Observed Complex0
Frequencyn/a


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