A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564782



Internal ID18765858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:81222163..81222414hg38UCSC Ensembl
Outerchr1:81222077..81222465hg38UCSC Ensembl
Innerchr1:81687848..81688099hg19UCSC Ensembl
Outerchr1:81687762..81688150hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763529
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564782
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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