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nsv4477506

  • 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: 102 SVs from 3 studies. See in: genome view    
Remapped(Score: Perfect):10,241,677-10,241,677Question Mark
Overlapping variant regions from other studies: 102 SVs from 3 studies. See in: genome view    
Submitted genomic10,241,789-10,241,789Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4477506RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr510,241,67710,241,677
nsv4477506Submitted genomicGRCh37.p13Primary AssemblyNC_000005.9Chr510,241,78910,241,789

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16058872alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16058872RemappedPerfectNC_000005.10:g.102
41677_10241678ins1
16
GRCh38.p12First PassNC_000005.10Chr510,241,67710,241,677
nssv16058872Submitted genomicNC_000005.9:g.1024
1789_10241790ins11
6
GRCh37.p13NC_000005.9Chr510,241,78910,241,789

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)
nssv160588724.6e-005121694
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