A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546674



Internal ID18747750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:91209473..91209786hg38UCSC Ensembl
Outerchr10:91209399..91209828hg38UCSC Ensembl
Innerchr10:92969230..92969543hg19UCSC Ensembl
Outerchr10:92969156..92969585hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9745421
Samples
Known GenesPCGF5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546674
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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