A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1958n100



Internal ID22788045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94170777..94277392hg38UCSC Ensembl
chr14:94637114..94743729hg19UCSC Ensembl
chr14:93706867..93813482hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38106616
hg19106616
hg18106616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1039901, nsv1045818, nsv1049719, nsv1055048, nsv1052876, nsv1040223
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)dgv1958n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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