A curated catalogue of human genomic structural variation

Variant Details

Variant: esv7871

Internal ID9605139
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:226978463..226978840hg38UCSC Ensembl
Outerchr1:226978411..226978893hg38UCSC Ensembl
Innerchr1:227166164..227166541hg19UCSC Ensembl
Outerchr1:227166112..227166594hg19UCSC Ensembl
Innerchr1:225232787..225233164hg18UCSC Ensembl
Outerchr1:225232735..225233217hg18UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv30312
Known GenesADCK3
AnalysisWe detected SVs based on span size and orientation information of each paired-end read. Paired-end reads with an anomalously long span size (more than double the average span size of each DNA library) were identified as SV candidates (deletion and inversion), especially when they had a minimum of three reads in the region, maximum 100 read depth and mapping quality (Q20). SV candidates either found in repeat regions of the genome or having more than 100 kb of genomic deletions were filtered out. For insertion detection larger than the short indels (-29 to +14 bp), the longest 300-bp span size of our paired-end libraries was used. Thus, we could fill 175-bp to 250-bp insert gaps between short inserts and large inserts. The criteria used for detecting these insertions absent from the reference genome in the range of 175-250 bp were minimum four read depth, maximum 60 read depth to filter out randomly placed hits in a repetitive structure region, and mapping quality (Q20).
PlatformIllumina Genome Analyzer
Pubmed ID19470904
Accession Number(s)esv7871
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0

Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer