A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv854n100



Internal ID22786941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52757467..52785830hg38UCSC Ensembl
chr10:54517227..54545590hg19UCSC Ensembl
chr10:54187233..54215596hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3828364
hg1928364
hg1828364
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1042522, nsv1042037
Samples
Known GenesMBL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv854n100
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