A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9741283



Internal ID18368843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141913801..141913861hg38UCSC Ensembl
chr7:141613601..141613661hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3542536
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9741283
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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