A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv801n100



Internal ID20152417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46407438..46489856hg38UCSC Ensembl
chr10:47046997..47142310hg19UCSC Ensembl
chr10:46467003..46562316hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3882419
hg1995314
hg1895314
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035412, nsv1047259, nsv1051440, nsv1052689, nsv1040814
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)dgv801n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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