A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9763913



Internal ID18738159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184257342..184257410hg38UCSC Ensembl
chr4:185178495..185178563hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3565166
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9763913
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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