A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv722n100



Internal ID22786809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42954840..42992538hg38UCSC Ensembl
chr10:43450288..43487986hg19UCSC Ensembl
chr10:42770294..42807992hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3837699
hg1937699
hg1837699
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041825, nsv1047289, nsv1054655
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)dgv722n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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