A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv792n100



Internal ID22786879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47025092..47392320hg19UCSC Ensembl
chr10:46445098..46812326hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19367229
hg18367229
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053674, nsv1047946, nsv1045436, nsv1051824, nsv1050877, nsv1040139, nsv1050502, nsv1041334, nsv1047464, nsv1053077, nsv1035923, nsv1054346, nsv1036902, nsv1038252, nsv1050330, nsv1049896, nsv1048900, nsv1042276
Samples
Known GenesAGAP9, ANXA8, BMS1P2, BMS1P6, FAM25C, FAM25G, FAM35DP, HNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv792n100
Frequency
Sample Size11257
Observed Gain83
Observed Loss45
Observed Complex0
Frequencyn/a


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