A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv693n100



Internal ID22786780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24554857..24574091hg38UCSC Ensembl
chr10:24843786..24863020hg19UCSC Ensembl
chr10:24883792..24903026hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3819235
hg1919235
hg1819235
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1042256, nsv1053560
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)dgv693n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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