A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv409e59



Internal ID20127158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46399419..46597271hg38UCSC Ensembl
chr10:46952346..47150344hg19UCSC Ensembl
chr10:46372352..46570350hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38197853
hg19197999
hg18197999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3345301, esv3343580, esv3408497
SamplesNA19239, NA19238, NA19240
Known GenesGPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R, SYT15
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv409e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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