A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv753n100



Internal ID19011121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46395843..46631445hg38UCSC Ensembl
chr10:46918172..47153919hg19UCSC Ensembl
chr10:46338178..46573925hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38235603
hg19235748
hg18235748
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053859, nsv1055032, nsv1043728, nsv1053359, nsv1047857, nsv1050886, nsv1046953, nsv1037662, nsv1046287, nsv1050501
Samples
Known GenesFAM35BP, GPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv753n100
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