A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9740940



Internal ID18715186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:102848274..102848593hg38UCSC Ensembl
Outerchr7:102848193..102848636hg38UCSC Ensembl
Innerchr7:102488721..102489040hg19UCSC Ensembl
Outerchr7:102488640..102489083hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3542193
Supporting Variants
Samples
Known GenesFBXL13
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9740940
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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