A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9745822



Internal ID18720068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:131111120..131114395hg38UCSC Ensembl
Outerchr10:131110688..131114898hg38UCSC Ensembl
Innerchr10:132909383..132912658hg19UCSC Ensembl
Outerchr10:132908951..132913161hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg384211
hg194211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3547075
Supporting Variants
Samples
Known GenesTCERG1L
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9745822
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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