nsv4558800

  • 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: 41 SVs from 2 studies. See in: genome view    
Remapped(Score: Perfect):123,496,818-123,496,818Question Mark
Overlapping variant regions from other studies: 41 SVs from 2 studies. See in: genome view    
Submitted genomic124,509,058-124,509,058Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4558800RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8123,496,818123,496,818
nsv4558800Submitted genomicGRCh37.p13Primary AssemblyNC_000008.10Chr8124,509,058124,509,058

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16083012sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16083012RemappedPerfectNC_000008.11:g.123
496818_123496819in
s1288
GRCh38.p12First PassNC_000008.11Chr8123,496,818123,496,818
nssv16083012Submitted genomicNC_000008.10:g.124
509058_124509059in
s1288
GRCh37.p13NC_000008.10Chr8124,509,058124,509,058

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)
nssv160830124.7e-005121490
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