A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9745219



Internal ID18372779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:69409867..69409919hg38UCSC Ensembl
Outerchr10:69409865..69409921hg38UCSC Ensembl
Innerchr10:71169623..71169675hg19UCSC Ensembl
Outerchr10:71169621..71169677hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3546472
Supporting Variants
Samples
Known GenesTACR2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9745219
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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