A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564176



Internal ID16004899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:30896678..30944286hg38UCSC Ensembl
Innerchr14:31365884..31413492hg19UCSC Ensembl
Innerchr14:30435635..30483243hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3847609
hg1947609
hg1847609
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3605n54
Supporting Variantsnssv825141
Samples
Known GenesSTRN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564176
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