A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546693



Internal ID18747769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:93282351..93285412hg38UCSC Ensembl
Outerchr10:93281459..93286105hg38UCSC Ensembl
Innerchr10:95042108..95045169hg19UCSC Ensembl
Outerchr10:95041216..95045862hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg384647
hg194647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9745440
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546693
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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