A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9755383



Internal ID18729629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54959220..54960615hg38UCSC Ensembl
Outerchr19:54959092..54960817hg38UCSC Ensembl
Innerchr19:55470588..55471983hg19UCSC Ensembl
Outerchr19:55470460..55472185hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg381726
hg191726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3556636
Supporting Variants
Samples
Known GenesRNU6-35P, RNU6-64P
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9755383
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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