A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1418887



Internal ID15235941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:38084561..38084781hg38UCSC Ensembl
Outerchr3:38126052..38126272hg19UCSC Ensembl
Outerchr3:38101056..38101276hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg381744
hg191744
hg181744
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv820288
Supporting Variants
SamplesAK1
Known GenesDLEC1
MethodSequencing
AnalysisCNV insertion could be detected in Long Insert sized Paired End (LIPE) data on the basis of compressed pairs which indicated insertion of certain sequence between pair reads. The average insert size of the LIPE library was 2,700 bp and the standard deviation (SD) was about 300 bp. Based on these figures, a compressed pair was defined as one with insert size shorter than 2,000 bp (< mean - 2 SD). Similar to method used to detect deletion, compressed pairs were defined to be clustered if one compressed pair was within 3,300 bp (mean + 2 SD) to neighboring compressed pair. To remove redundant pairs present in LIPE library, two or more pairs with both reads aligned to exactly the same position of reference genome were defined as one pair and named de-redundant. If 10 or more deredundant compressed pairs were found in one cluster, we defined this region as a candidate region for amplification.
PlatformGPL10329
Comments
ReferenceKim_et_al_2009
Pubmed ID19587683
Accession Number(s)nssv1418887
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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