A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9765569



Internal ID18739815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:152381371..152381658hg38UCSC Ensembl
Outerchr5:152381323..152381709hg38UCSC Ensembl
Innerchr5:151760932..151761219hg19UCSC Ensembl
Outerchr5:151760884..151761270hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3566822
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9765569
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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