A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546774



Internal ID18401164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:103337834..103338049hg38UCSC Ensembl
Outerchr10:103337765..103338095hg38UCSC Ensembl
Innerchr10:105097591..105097806hg19UCSC Ensembl
Outerchr10:105097522..105097852hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv39e215
Supporting Variantsessv9745521
Samples
Known GenesPCGF6
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546774
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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