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nsv4573467

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 53 SVs from 11 studies. See in: genome view    
Remapped(Score: Perfect):180,672,801-180,672,801Question Mark
Overlapping variant regions from other studies: 53 SVs from 11 studies. See in: genome view    
Submitted genomic180,641,937-180,641,937Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4573467RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1180,672,801180,672,801
nsv4573467Submitted genomicGRCh37.p13Primary AssemblyNC_000001.10Chr1180,641,937180,641,937

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16026694line1 insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16026694RemappedPerfectNC_000001.11:g.180
672801_180672802in
s780
GRCh38.p12First PassNC_000001.11Chr1180,672,801180,672,801
nssv16026694Submitted genomicNC_000001.10:g.180
641937_180641938in
s780
GRCh37.p13NC_000001.10Chr1180,641,937180,641,937

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)
nssv160266940.0036921676
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