A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1967n100



Internal ID22788054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98568588..98592611hg38UCSC Ensembl
chr14:99034925..99058948hg19UCSC Ensembl
chr14:98104678..98128701hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3824024
hg1924024
hg1824024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040824, nsv1045975, nsv1039423
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1967n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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