A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3556695



Internal ID18757771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:58319428..58322131hg38UCSC Ensembl
Outerchr19:58319330..58322367hg38UCSC Ensembl
Innerchr19:58830794..58833497hg19UCSC Ensembl
Outerchr19:58830696..58833733hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg383038
hg193038
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9755442
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3556695
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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