A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573819



Internal ID16014542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89907493..89908286hg38UCSC Ensembl
Innerchr16:89973901..89974694hg19UCSC Ensembl
Innerchr16:88501402..88502195hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38794
hg19794
hg18794
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5338n54
Supporting Variantsnssv863733, nssv863732, nssv863727, nssv863728, nssv863729, nssv863734, nssv863736, nssv863730, nssv863731, nssv863735, nssv863726
Samples
Known GenesTCF25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573819
Frequency
Sample Size17421
Observed Gain9
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer