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nsv5408241

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:43

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 100 SVs from 24 studies. See in: genome view    
Submitted genomic143,662,598-143,662,640Question Mark
Overlapping variant regions from other studies: 100 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):143,983,735-143,983,777Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5408241Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6143,662,598143,662,640
nsv5408241RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6143,983,735143,983,777

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16971226alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16971226Submitted genomicNC_000006.12:g.143
662598_143662640in
s281
GRCh38 (hg38)NC_000006.12Chr6143,662,598143,662,640
nssv16971226RemappedPerfectNC_000006.11:g.143
983735_143983777in
s281
GRCh37.p13First PassNC_000006.11Chr6143,983,735143,983,777

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)
nssv169712260.003206404
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