A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv743n100



Internal ID19011111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46411170..46878295hg38UCSC Ensembl
chr10:46674168..47138582hg19UCSC Ensembl
chr10:46094174..46558588hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38467126
hg19464415
hg18464415
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1055017, nsv1040108, nsv1045185, nsv1039765, nsv1035291, nsv1041036, nsv1046669, nsv1052440, nsv1045770, nsv1045328, nsv1044607, nsv1050198, nsv1050384, nsv1055118, nsv1044415, nsv1051267
Samples
Known GenesBMS1P1, BMS1P5, FAM35BP, FRMPD2P1, GLUD1P7, 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)dgv743n100
Frequency
Sample Size29084
Observed Gain24
Observed Loss0
Observed Complex0
Frequencyn/a


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