A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv740n100



Internal ID19011108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46407438..46962260hg38UCSC Ensembl
chr10:46590219..47142310hg19UCSC Ensembl
chr10:46010225..46562316hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38554823
hg19552092
hg18552092
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048332, nsv1048338, nsv1037395, nsv1052860, nsv1036520, nsv1046798, nsv1047029, nsv1045049, nsv1041893
Samples
Known GenesBMS1P1, BMS1P5, FAM35BP, FRMPD2P1, GLUD1P7, GPRIN2, HNRNPA1P33, 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)dgv740n100
Frequency
Sample Size29084
Observed Gain32
Observed Loss14
Observed Complex0
Frequencyn/a


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