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nsv5542553

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:49

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 127 SVs from 29 studies. See in: genome view    
Submitted genomic94,122,803-94,122,851Question Mark
Overlapping variant regions from other studies: 127 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):95,043,954-95,044,002Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5542553Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr494,122,80394,122,851
nsv5542553RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr495,043,95495,044,002

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16952773insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16952773Submitted genomicNC_000004.12:g.941
22803_94122851ins1
00
GRCh38 (hg38)NC_000004.12Chr494,122,80394,122,851
nssv16952773RemappedPerfectNC_000004.11:g.950
43954_95044002ins1
00
GRCh37.p13First PassNC_000004.11Chr495,043,95495,044,002

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)
nssv16952773<0.00136404
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