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nsv4060698

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:359,528

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 681 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):189,270,747-189,630,274Question Mark
Overlapping variant regions from other studies: 681 SVs from 20 studies. See in: genome view    
Submitted genomic189,239,878-189,599,404Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4060698RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1189,270,747189,630,274
nsv4060698Submitted genomicGRCh37.p13Primary AssemblyNC_000001.10Chr1189,239,878189,599,404

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15847182deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15847182RemappedPerfectNC_000001.11:g.189
270747_189630274de
l
GRCh38.p12First PassNC_000001.11Chr1189,270,747189,630,274
nssv15847182Submitted genomicNC_000001.10:g.189
239878_189599404de
l
GRCh37.p13NC_000001.10Chr1189,239,878189,599,404

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)
nssv158471820.0012421694
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