A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9763882



Internal ID18738128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:182815219..182815402hg38UCSC Ensembl
Outerchr4:182815202..182815441hg38UCSC Ensembl
Innerchr4:183736372..183736555hg19UCSC Ensembl
Outerchr4:183736355..183736594hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3565135
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9763882
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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