A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637147



Internal ID7023941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86985783..86986612hg38UCSC Ensembl
Innerchr15:86985783..86986612hg38UCSC Ensembl
Outerchr15:86985522..86986918hg38UCSC Ensembl
chr15:87529014..87529843hg19UCSC Ensembl
Innerchr15:87529014..87529843hg19UCSC Ensembl
Outerchr15:87528753..87530149hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38830
hg19830
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15315950, essv15315951
SamplesNA19446, NA19445
Known GenesAGBL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637147
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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