A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564615



Internal ID18765691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:79648515..79648780hg38UCSC Ensembl
Outerchr1:79648453..79648847hg38UCSC Ensembl
Innerchr1:80114200..80114465hg19UCSC Ensembl
Outerchr1:80114138..80114532hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38395
hg19395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763362
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564615
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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