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nsv4501127

  • 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: 39 SVs from 8 studies. See in: genome view    
Remapped(Score: Perfect):77,304,319-77,304,319Question Mark
Overlapping variant regions from other studies: 39 SVs from 8 studies. See in: genome view    
Submitted genomic77,770,662-77,770,662Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4501127RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000014.9Chr1477,304,31977,304,319
nsv4501127Submitted genomicGRCh37.p13Primary AssemblyNC_000014.8Chr1477,770,66277,770,662

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16011051alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16011051RemappedPerfectNC_000014.9:g.7730
4319_77304320ins28
0
GRCh38.p12First PassNC_000014.9Chr1477,304,31977,304,319
nssv16011051Submitted genomicNC_000014.8:g.7777
0662_77770663ins28
0
GRCh37.p13NC_000014.8Chr1477,770,66277,770,662

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)
nssv16011051<0.001321694
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