nsv4565485

  • 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):123,522,088-123,522,088Question Mark
Overlapping variant regions from other studies: 41 SVs from 2 studies. See in: genome view    
Submitted genomic124,534,328-124,534,328Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4565485RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8123,522,088123,522,088
nsv4565485Submitted genomicGRCh37.p13Primary AssemblyNC_000008.10Chr8124,534,328124,534,328

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16083013line1 insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16083013RemappedPerfectNC_000008.11:g.123
522088_123522089in
s659
GRCh38.p12First PassNC_000008.11Chr8123,522,088123,522,088
nssv16083013Submitted genomicNC_000008.10:g.124
534328_124534329in
s659
GRCh37.p13NC_000008.10Chr8124,534,328124,534,328

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)
nssv16083013<0.001621690
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