A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637189



Internal ID7023983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89286055..89287040hg38UCSC Ensembl
Innerchr15:89286103..89286992hg38UCSC Ensembl
Outerchr15:89286007..89287088hg38UCSC Ensembl
chr15:89829286..89830271hg19UCSC Ensembl
Innerchr15:89829334..89830223hg19UCSC Ensembl
Outerchr15:89829238..89830319hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38986
hg19986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15317071
SamplesHG02006
Known GenesFANCI
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637189
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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