A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039901



Internal ID19129120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:94170777..94254190hg38UCSC Ensembl
Innerchr14:94637114..94720527hg19UCSC Ensembl
Innerchr14:93706867..93790280hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3883414
hg1983414
hg1883414
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1958n100
Supporting Variantsnssv3532600
Samples
Known GenesPPP4R4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039901
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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