A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636415



Internal ID6676522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48397504..48409161hg38UCSC Ensembl
Innerchr15:48397504..48409161hg38UCSC Ensembl
Outerchr15:48397004..48409661hg38UCSC Ensembl
chr15:48689701..48701358hg19UCSC Ensembl
Innerchr15:48689701..48701358hg19UCSC Ensembl
Outerchr15:48689201..48701858hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3811658
hg1911658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15243874
SamplesNA19159
Known GenesFBN1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636415
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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