A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751696



Internal ID18725942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101213622..101216209hg38UCSC Ensembl
Outerchr15:101213271..101216418hg38UCSC Ensembl
Innerchr15:101753827..101756414hg19UCSC Ensembl
Outerchr15:101753476..101756623hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg383148
hg193148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552949
Supporting Variants
Samples
Known GenesCHSY1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751696
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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