A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9755446



Internal ID18729692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:58504520..58506108hg38UCSC Ensembl
Outerchr19:58504326..58506406hg38UCSC Ensembl
Innerchr19:59015887..59017475hg19UCSC Ensembl
Outerchr19:59015693..59017773hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg382081
hg192081
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3556699
Supporting Variants
Samples
Known GenesSLC27A5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9755446
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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