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nsv5489859

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:83

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 104 SVs from 20 studies. See in: genome view    
Submitted genomic104,124,293-104,124,375Question Mark
Overlapping variant regions from other studies: 104 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):106,886,574-106,886,656Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5489859Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9104,124,293104,124,375
nsv5489859RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9106,886,574106,886,656

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17027045deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17027045Submitted genomicNC_000009.12:g.104
124293_104124375de
l
GRCh38 (hg38)NC_000009.12Chr9104,124,293104,124,375
nssv17027045RemappedPerfectNC_000009.11:g.106
886574_106886656de
l
GRCh37.p13First PassNC_000009.11Chr9106,886,574106,886,656

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)
nssv17027045<0.00116404
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