A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv752n100



Internal ID19011120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46401133..46631445hg38UCSC Ensembl
chr10:46918172..47148630hg19UCSC Ensembl
chr10:46338178..46568636hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38230313
hg19230459
hg18230459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054213, nsv1042335
Samples
Known GenesFAM35BP, 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)dgv752n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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