A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9765857



Internal ID18393417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:179915153..179917290hg38UCSC Ensembl
Outerchr5:179915027..179917311hg38UCSC Ensembl
Innerchr5:179342153..179344290hg19UCSC Ensembl
Outerchr5:179342027..179344311hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg382285
hg192285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3567110
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9765857
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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