A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3556441



Internal ID18757517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43822585..43822749hg38UCSC Ensembl
Outerchr19:43822570..43822769hg38UCSC Ensembl
Innerchr19:44326737..44326901hg19UCSC Ensembl
Outerchr19:44326722..44326921hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9755188
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3556441
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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