A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv689n100



Internal ID22786776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24083364..24102024hg38UCSC Ensembl
chr10:24372293..24390953hg19UCSC Ensembl
chr10:24412299..24430959hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3818661
hg1918661
hg1818661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038805, nsv1038178
Samples
Known GenesKIAA1217
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv689n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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