A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637201



Internal ID6677308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89678659..89694358hg38UCSC Ensembl
Innerchr15:89678659..89694358hg38UCSC Ensembl
Outerchr15:89678159..89694858hg38UCSC Ensembl
chr15:90221890..90237589hg19UCSC Ensembl
Innerchr15:90221890..90237589hg19UCSC Ensembl
Outerchr15:90221390..90238089hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3815700
hg1915700
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15317176
SamplesHG03969
Known GenesPEX11A, PLIN1, WDR93
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637201
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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