A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546628



Internal ID18747704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87516052..87516797hg38UCSC Ensembl
Outerchr10:87515939..87516938hg38UCSC Ensembl
Innerchr10:89275809..89276554hg19UCSC Ensembl
Outerchr10:89275696..89276695hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9745375
Samples
Known GenesMINPP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546628
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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