A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637137



Internal ID7023931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86402782..86403588hg38UCSC Ensembl
Innerchr15:86402782..86403588hg38UCSC Ensembl
Outerchr15:86402709..86403668hg38UCSC Ensembl
chr15:86946013..86946819hg19UCSC Ensembl
Innerchr15:86946013..86946819hg19UCSC Ensembl
Outerchr15:86945940..86946899hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38807
hg19807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15315910
SamplesNA19403
Known GenesAGBL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637137
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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