A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9762652



Internal ID18736898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:58301763..58313690hg38UCSC Ensembl
Outerchr4:58298881..58317058hg38UCSC Ensembl
Innerchr4:59167929..59179856hg19UCSC Ensembl
Outerchr4:59165047..59183224hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3818178
hg1918178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3563905
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9762652
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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