A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv813n100



Internal ID20152429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46407438..46489856hg38UCSC Ensembl
chr10:47058887..47142310hg19UCSC Ensembl
chr10:46478893..46562316hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3882419
hg1983424
hg1883424
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038585, nsv1054923, nsv1046805, nsv1044151, nsv1043498, nsv1041386, nsv1035250, nsv1037446
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)dgv813n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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