A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9745716



Internal ID18719962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122457333..122457660hg38UCSC Ensembl
Outerchr10:122457284..122457746hg38UCSC Ensembl
Innerchr10:124216849..124217176hg19UCSC Ensembl
Outerchr10:124216800..124217262hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3546969
Supporting Variants
Samples
Known GenesARMS2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9745716
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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