A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9755300



Internal ID18729546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51402178..51402358hg38UCSC Ensembl
Outerchr19:51402163..51402374hg38UCSC Ensembl
Innerchr19:51905432..51905612hg19UCSC Ensembl
Outerchr19:51905417..51905628hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3556553
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9755300
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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