A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv39e215



Internal ID20151078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103337718..103338104hg38UCSC Ensembl
chr10:105097475..105097861hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3546774, esv3546775
Samples
Known GenesPCGF6
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)dgv39e215
Frequency
Sample Size767
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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