A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv834n100



Internal ID20152450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46169941..46332377hg38UCSC Ensembl
chr10:47541177..47703613hg19UCSC Ensembl
chr10:47011183..47173619hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38162437
hg19162437
hg18162437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046794, nsv1052572
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv834n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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