A curated catalogue of human genomic structural variation




Variant Details

Variant: esv7859



Internal ID9605127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:56776953..56777282hg38UCSC Ensembl
Outerchr1:56776714..56777533hg38UCSC Ensembl
Innerchr1:57242626..57242955hg19UCSC Ensembl
Outerchr1:57242387..57243206hg19UCSC Ensembl
Innerchr1:57015214..57015543hg18UCSC Ensembl
Outerchr1:57014975..57015794hg18UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38820
hg19820
hg18820
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv30300
Samples
Known GenesC1orf168
MethodSequencing
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
Comments
ReferenceAhn_et_al_2009
Pubmed ID19470904
Accession Number(s)esv7859
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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