A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546767



Internal ID18747843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:102885504..102885794hg38UCSC Ensembl
Outerchr10:102885433..102885866hg38UCSC Ensembl
Innerchr10:104645261..104645551hg19UCSC Ensembl
Outerchr10:104645190..104645623hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9745514
Samples
Known GenesAS3MT, C10orf32-ASMT
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546767
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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