A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751655



Internal ID18725901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:98162878..98163154hg38UCSC Ensembl
Outerchr15:98162843..98163217hg38UCSC Ensembl
Innerchr15:98706107..98706383hg19UCSC Ensembl
Outerchr15:98706072..98706446hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552908
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751655
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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