A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9759717



Internal ID18733963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:38137102..38139036hg38UCSC Ensembl
Outerchr1:38136738..38139175hg38UCSC Ensembl
Innerchr1:38602774..38604708hg19UCSC Ensembl
Outerchr1:38602410..38604847hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg382438
hg192438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3560970
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9759717
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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