A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9763423



Internal ID18737669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:135167590..135172857hg38UCSC Ensembl
Outerchr4:135167236..135173165hg38UCSC Ensembl
Innerchr4:136088745..136094012hg19UCSC Ensembl
Outerchr4:136088391..136094320hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg385930
hg195930
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3564676
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9763423
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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