A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751574



Internal ID18379134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89516520..89518523hg38UCSC Ensembl
Outerchr15:89516126..89518554hg38UCSC Ensembl
Innerchr15:90059751..90061754hg19UCSC Ensembl
Outerchr15:90059357..90061785hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382429
hg192429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552827
Supporting Variants
Samples
Known GenesLINC00928
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751574
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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