A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3565259



Internal ID18766335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:85282977..85283234hg38UCSC Ensembl
Outerchr1:85282916..85283306hg38UCSC Ensembl
Innerchr1:85748660..85748917hg19UCSC Ensembl
Outerchr1:85748599..85748989hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9764006
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3565259
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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