A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3554088



Internal ID18408478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:26599922..26600215hg38UCSC Ensembl
Outerchr2:26599868..26600266hg38UCSC Ensembl
Innerchr2:26822790..26823083hg19UCSC Ensembl
Outerchr2:26822736..26823134hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9752835
Samples
Known GenesCIB4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3554088
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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