A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9754618



Internal ID18728864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:3011307..3011578hg38UCSC Ensembl
Outerchr19:3011279..3011603hg38UCSC Ensembl
Innerchr19:3011305..3011576hg19UCSC Ensembl
Outerchr19:3011277..3011601hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3555871
Supporting Variants
Samples
Known GenesTLE2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9754618
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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