A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9745457



Internal ID18719703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:95447299..95448270hg38UCSC Ensembl
Outerchr10:95447276..95448434hg38UCSC Ensembl
Innerchr10:97207056..97208027hg19UCSC Ensembl
Outerchr10:97207033..97208191hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg381159
hg191159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3546710
Supporting Variants
Samples
Known GenesSORBS1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9745457
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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