A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2665n100



Internal ID22788752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94233701..94285021hg38UCSC Ensembl
chr15:94776930..94828250hg19UCSC Ensembl
chr15:92577934..92629254hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3851321
hg1951321
hg1851321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046758, nsv1046954, nsv1053735, nsv1048518, nsv1053984, nsv1042975
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)dgv2665n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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