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nsv5539948

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:274

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 99 SVs from 19 studies. See in: genome view    
Submitted genomic131,404,795-131,405,068Question Mark
Overlapping variant regions from other studies: 99 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):131,725,935-131,726,208Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5539948Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6131,404,795131,405,068
nsv5539948RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6131,725,935131,726,208

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16969131insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16969131Submitted genomicNC_000006.12:g.131
404795_131405068in
s271
GRCh38 (hg38)NC_000006.12Chr6131,404,795131,405,068
nssv16969131RemappedPerfectNC_000006.11:g.131
725935_131726208in
s271
GRCh37.p13First PassNC_000006.11Chr6131,725,935131,726,208

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)
nssv16969131<0.00146398
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