A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv751n100



Internal ID20152367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46467768..46631445hg38UCSC Ensembl
chr10:46918172..47081683hg19UCSC Ensembl
chr10:46338178..46501689hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38163678
hg19163512
hg18163512
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044141, nsv1049466, nsv1053170, nsv1037751, nsv1046194, nsv1050275, nsv1048058
Samples
Known GenesFAM35BP, GPRIN2, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv751n100
Frequency
Sample Size29084
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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