A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv812n100



Internal ID20152428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46395843..46489856hg38UCSC Ensembl
chr10:47058780..47153919hg19UCSC Ensembl
chr10:46478786..46573925hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3894014
hg1995140
hg1895140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037371, nsv1053331, nsv1038077, nsv1048658, nsv1048712, nsv1052534, nsv1038700, nsv1037347, nsv1045031, nsv1054598, nsv1054931, nsv1052680, nsv1044274, nsv1036538, nsv1047286
Samples
Known GenesHNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv812n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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