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nsv4489407

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 30 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):122,418,285-122,418,285Question Mark
Overlapping variant regions from other studies: 30 SVs from 5 studies. See in: genome view    
Submitted genomic122,739,430-122,739,430Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4489407RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6122,418,285122,418,285
nsv4489407Submitted genomicGRCh37.p13Primary AssemblyNC_000006.11Chr6122,739,430122,739,430

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16071675alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16071675RemappedPerfectNC_000006.12:g.122
418285_122418286in
s280
GRCh38.p12First PassNC_000006.12Chr6122,418,285122,418,285
nssv16071675Submitted genomicNC_000006.11:g.122
739430_122739431in
s280
GRCh37.p13NC_000006.11Chr6122,739,430122,739,430

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)
nssv160716754.6e-005121694
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