A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9762202



Internal ID18736448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:14680050..14682018hg38UCSC Ensembl
Outerchr4:14680028..14682092hg38UCSC Ensembl
Innerchr4:14681674..14683642hg19UCSC Ensembl
Outerchr4:14681652..14683716hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg382065
hg192065
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3563455
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9762202
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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