A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9755297



Internal ID18729543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51273219..51273425hg38UCSC Ensembl
Outerchr19:51273133..51273504hg38UCSC Ensembl
Innerchr19:51776473..51776679hg19UCSC Ensembl
Outerchr19:51776387..51776758hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3556550
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9755297
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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