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nsv4481893

  • 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: 48 SVs from 4 studies. See in: genome view    
Remapped(Score: Perfect):68,543,960-68,543,960Question Mark
Overlapping variant regions from other studies: 48 SVs from 3 studies. See in: genome view    
Submitted genomic71,158,876-71,158,876Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4481893RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr968,543,96068,543,960
nsv4481893Submitted genomicGRCh37.p13Primary AssemblyNC_000009.11Chr971,158,87671,158,876

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16084780alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16084780RemappedPerfectNC_000009.12:g.685
43960_68543961ins2
81
GRCh38.p12First PassNC_000009.12Chr968,543,96068,543,960
nssv16084780Submitted genomicNC_000009.11:g.711
58876_71158877ins2
81
GRCh37.p13NC_000009.11Chr971,158,87671,158,876

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)
nssv160847804.6e-005121694
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