A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv738n100



Internal ID19011106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46395843..47008602hg38UCSC Ensembl
chr10:46543845..47153919hg19UCSC Ensembl
chr10:45963851..46573925hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38612760
hg19610075
hg18610075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1039063, nsv1035520, nsv1052359
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)dgv738n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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