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nsv5513455

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:141

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 191 SVs from 19 studies. See in: genome view    
Submitted genomic106,505,523-106,505,663Question Mark
Overlapping variant regions from other studies: 191 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):107,157,871-107,158,011Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5513455Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr13106,505,523106,505,663
nsv5513455RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr13107,157,871107,158,011

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17692325duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17692325Submitted genomicNC_000013.11:g.106
505523_106505663du
p
GRCh38 (hg38)NC_000013.11Chr13106,505,523106,505,663
nssv17692325RemappedPerfectNC_000013.10:g.107
157871_107158011du
p
GRCh37.p13First PassNC_000013.10Chr13107,157,871107,158,011

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17692325<0.00116404
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