A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9745789



Internal ID18720035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:128137319..128137606hg38UCSC Ensembl
Outerchr10:128137273..128137672hg38UCSC Ensembl
Innerchr10:129935583..129935870hg19UCSC Ensembl
Outerchr10:129935537..129935936hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3547042
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9745789
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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