A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751688



Internal ID18725934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100511580..100511971hg38UCSC Ensembl
Outerchr15:100511510..100512079hg38UCSC Ensembl
Innerchr15:101051785..101052176hg19UCSC Ensembl
Outerchr15:101051715..101052284hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38570
hg19570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552941
Supporting Variants
Samples
Known GenesCERS3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751688
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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