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nsv5561376

  • 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: 128 SVs from 45 studies. See in: genome view    
Submitted genomic57,423,045-57,423,096Question Mark
Overlapping variant regions from other studies: 196 SVs from 56 studies. See in: genome view    
Remapped(Score: Perfect):57,287,843-57,287,894Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5561376Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr657,423,04557,423,096
nsv5561376RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr657,287,84357,287,894

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16983405line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16983405Submitted genomicNC_000006.12:g.574
23045_57423096ins6
013
GRCh38 (hg38)NC_000006.12Chr657,423,04557,423,096
nssv16983405RemappedPerfectNC_000006.11:g.572
87843_57287894ins6
013
GRCh37.p13First PassNC_000006.11Chr657,287,84357,287,894

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)
nssv16983405<0.00126404
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