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nsv5407030

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 280 SVs from 31 studies. See in: genome view    
Submitted genomic134,397,517-134,397,568Question Mark
Overlapping variant regions from other studies: 268 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):137,289,363-137,289,414Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5407030Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9134,397,517134,397,568
nsv5407030RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9137,289,363137,289,414

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17031134alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17031134Submitted genomicNC_000009.12:g.134
397517_134397568in
s280
GRCh38 (hg38)NC_000009.12Chr9134,397,517134,397,568
nssv17031134RemappedPerfectNC_000009.11:g.137
289363_137289414in
s280
GRCh37.p13First PassNC_000009.11Chr9137,289,363137,289,414

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)
nssv170311340.002136404
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