A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546861



Internal ID18401251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:112398042..112398326hg38UCSC Ensembl
Outerchr10:112398017..112398392hg38UCSC Ensembl
Innerchr10:114157800..114158084hg19UCSC Ensembl
Outerchr10:114157775..114158150hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9745608
Samples
Known GenesACSL5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546861
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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