A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566057



Internal ID16006780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104680242..104844912hg38UCSC Ensembl
Innerchr14:105146579..105311249hg19UCSC Ensembl
Innerchr14:104217624..104382294hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38164671
hg19164671
hg18164671
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834438, nssv834439
Samples
Known GenesADSSL1, AKT1, INF2, LINC00638, SIVA1, ZBTB42
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566057
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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