A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv734n100



Internal ID19011102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46428386..47024352hg38UCSC Ensembl
chr10:46527665..47121369hg19UCSC Ensembl
chr10:45947671..46541375hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38595967
hg19593705
hg18593705
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037608, nsv1042761, nsv1039126, nsv1046239, nsv1053579, nsv1048865, nsv1054619, nsv1045466, nsv1039083, nsv1042036, nsv1036781, nsv1046493, nsv1053195, nsv1041896
Samples
Known GenesBMS1P1, BMS1P5, FAM35BP, FRMPD2P1, GLUD1P7, GPRIN2, LINC00842, LOC100996758, NPY4R, PTPN20A, PTPN20B, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv734n100
Frequency
Sample Size29084
Observed Gain17
Observed Loss0
Observed Complex0
Frequencyn/a


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