A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3556387



Internal ID18757463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39958402..39958973hg38UCSC Ensembl
Outerchr19:39958384..39959010hg38UCSC Ensembl
Innerchr19:40464309..40464880hg19UCSC Ensembl
Outerchr19:40464291..40464917hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9755134
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3556387
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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