A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566071



Internal ID16353480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104776494..104808426hg38UCSC Ensembl
Innerchr14:105242831..105274763hg19UCSC Ensembl
Innerchr14:104313876..104345808hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3831933
hg1931933
hg1831933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3957n54
Supporting Variantsnssv834452
Samples
Known GenesAKT1, ZBTB42
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566071
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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