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nsv5562075

  • 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 24 studies. See in: genome view    
Submitted genomic44,270,801-44,270,852Question Mark
Overlapping variant regions from other studies: 128 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):44,736,473-44,736,524Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5562075Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr144,270,80144,270,852
nsv5562075RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr144,736,47344,736,524

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16902558line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16902558Submitted genomicNC_000001.11:g.442
70801_44270852ins5
64
GRCh38 (hg38)NC_000001.11Chr144,270,80144,270,852
nssv16902558RemappedPerfectNC_000001.10:g.447
36473_44736524ins5
64
GRCh37.p13First PassNC_000001.10Chr144,736,47344,736,524

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)
nssv169025580.004246384
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