A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9745375



Internal ID18719621
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 StatusS
Merged Variantsesv3546628
Supporting Variants
Samples
Known GenesMINPP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9745375
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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