A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9762096



Internal ID18389656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:65798239..65798513hg38UCSC Ensembl
Outerchr1:65798193..65798581hg38UCSC Ensembl
Innerchr1:66263922..66264196hg19UCSC Ensembl
Outerchr1:66263876..66264264hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3563349
Supporting Variants
Samples
Known GenesPDE4B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9762096
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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