A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9753980



Internal ID18728226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:21363917..21364560hg38UCSC Ensembl
Outerchr1:21363898..21364624hg38UCSC Ensembl
Innerchr1:21690410..21691053hg19UCSC Ensembl
Outerchr1:21690391..21691117hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38727
hg19727
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3555233
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9753980
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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