A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3544566



Internal ID18745642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:10894367..10895940hg38UCSC Ensembl
Outerchr1:10894205..10896104hg38UCSC Ensembl
Innerchr1:10954424..10955997hg19UCSC Ensembl
Outerchr1:10954262..10956161hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9743313
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3544566
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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