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nsv4515918

  • 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: 33 SVs from 11 studies. See in: genome view    
Remapped(Score: Perfect):36,044,426-36,044,426Question Mark
Overlapping variant regions from other studies: 33 SVs from 11 studies. See in: genome view    
Submitted genomic36,535,328-36,535,328Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4515918RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000019.10Chr1936,044,42636,044,426
nsv4515918Submitted genomicGRCh37.p13Primary AssemblyNC_000019.9Chr1936,535,32836,535,328

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16023098alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16023098RemappedPerfectNC_000019.10:g.360
44426_36044427ins2
42
GRCh38.p12First PassNC_000019.10Chr1936,044,42636,044,426
nssv16023098Submitted genomicNC_000019.9:g.3653
5328_36535329ins24
2
GRCh37.p13NC_000019.9Chr1936,535,32836,535,328

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)
nssv160230980.0242221620
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